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TH Huisman

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Co-Publications
Name
61
Kutlar, Ferdane
48
Gu, LH
44
Kutlar, Abdullah
29
Molchanova, TP
28
Efremov, Georgi
20
Altay, Cigdem
19
Smetanina, NS
18
Adekile, Adekunle
16
Gurgey, Aytemiz
13
Oner, Cihan
12
Fei, You-Jun
10
Felice, Alex
10
Oner, Reyhan
9
Plaseska-Karanfilska, Dijana
8
Efremov, Dimitar

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Publications

TOP 3
Molchanova T P; Kolledey S V; Pronina L C; Mirgorodskaya O A; Musolyamov A C; Abaturov L V; Huisman T H
Unstable Hb Newcastle [beta92(F8)His-->Pro], first case discovered in a Russian patient.
Molchanova T P; Postnikov Yu V; Gu L H; Huisman T H
Historical note: the beta-thalassemia allele in the noble Russian family Lermontov is identified as the ATG-->ACG change in the initiation codon.
Huisman T H
A note about the relative elution rates of various abnormal hemoglobins and abnormal globin chains in cation exchange and reversed phase high performance liquid chromatography.

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All Publications

1999: Molchanova T P; Kolledey S V; Pronina L C; Mirgorodskaya O A; Musolyamov A C; Abaturov L V; Huisman T H
Unstable Hb Newcastle [beta92(F8)His-->Pro], first case discovered in a Russian patient.
Hemoglobin 1999;23(4):373-8.
1998: Molchanova T P; Postnikov Yu V; Gu L H; Huisman T H
Historical note: the beta-thalassemia allele in the noble Russian family Lermontov is identified as the ATG-->ACG change in the initiation codon.
Hemoglobin 1998;22(3):283-6.
1998: Huisman T H
A note about the relative elution rates of various abnormal hemoglobins and abnormal globin chains in cation exchange and reversed phase high performance liquid chromatography.
Hemoglobin 1998;22(3):267-72.
1998: Huisman T H; Carver M F
The beta- and delta-thalassemia repository (Ninth Edition; Part I).
Hemoglobin 1998;22(2):169-95.
1998: Hardison R C; Chui D H; Riemer C R; Miller W; Carver M F; Molchanova T P; Efremov G D; Huisman T H
Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web.
Hemoglobin 1998;22(2):113-27.
1998: Huisman T H; Carver M F
Recombinant hemoglobin variants.
Hemoglobin 1998;22(2):99-112.
1998: Hardison R; Riemer C; Chui D H; Huisman T H; Miller W
Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation.
Genomics 1998;47(3):429-37.
1998: Bissé E; Schlemer E; Lizama M; Huaman-Guillen P; Wieland H; Adam G; Molchanova T P; Huisman T H
Hb Strasbourg [beta 23(B5)Val-->Asp]; a high oxygen affinity variant observed in a German family.
Hemoglobin 1998;22(1):69-73.
1998: Smetanina N S; Gu L H; Huisman T H
Comparison of the relative quantities of gamma-mRNAs and fetal hemoglobin in SS patients with different haplotypes.
Acta haematologica 1998;100(1):4-8.
1997: Huisman T H
Combinations of beta chain abnormal hemoglobins with each other or with beta-thalassemia determinants with known mutations: influence on phenotype.
Clinical chemistry 1997;43(10):1850-6.
1997: Smetanina N S; Molchanova T P; Huisman T H
Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants.
Hemoglobin 1997;21(5):437-67.
1997: Huisman T H
Gamma chain abnormal human fetal hemoglobin variants.
American journal of hematology 1997;55(3):159-63.
1997: Ribeiro M L; Cunha E; Gonçalves P; Martin Núñez G; Fernandez Galan M A; Tamagnini G P; Smetanina N S; Gu L H; Huisman T H
Hb Lepore-Baltimore (delta 68Leu-beta 84Thr) and Hb Lepore-Washington-Boston (delta 87Gln-beta IVS-II-8) in central Portugal and Spanish Alta Extremadura.
Human genetics 1997;99(5):669-73.
1997: Huisman T H
Compound heterozygosity for Hb S and the hybrid HbS Lepore, P-Nilotic, and Kenya; comparison of hematological and hemoglobin composition data.
Hemoglobin 1997;21(3):249-57.
1997: Huisman T H
Hb E and alpha-thalassemia; variability in the assembly of beta E chain containing tetramers.
Hemoglobin 1997;21(3):227-36.
1997: Molchanova T P; Huisman T H
The levels of abnormal hemoglobin in persons with heterozygosities for an alpha chain variant and for beta-thalassemia.
Hemoglobin 1997;21(2):173-7.
1997: Okeagu J E; Smetanina N S; Huisman T H
Detection of the alpha-thalassemia-2 (3.7 kb) deletion in DNA extracted from 20-year-old blood smears.
Hemoglobin 1997;21(1):53-8.
1997: Smetanina N S; Gu L H; Simjanovska L; Momirovska A; Petkov G H; Adekile A D; Efremov G D; Huisman T H
Alpha-, beta-, and gamma-mRNA levels in beta-thalassemia; transcriptional and translational differences in heterozygotes, homozygotes, and compound heterozygotes.
Hemoglobin 1997;21(1):27-39.
1997: Huisman T H
Levels of Hb A2 in heterozygotes and homozygotes for beta-thalassemia mutations: influence of mutations in the CACCC and ATAAA motifs of the beta-globin gene promoter.
Acta haematologica 1997;98(4):187-94.
1997: Saleh A W; Velvis H J; Gu L H; Hillen H F; Huisman T H
Hydroxyurea therapy in sickle cell anemia patients in Curaçao, The Netherlands Antilles.
Acta haematologica 1997;98(3):125-9.
1997: Smetanina N S; Gu L H; Schilirò G; Di Cataldo A; Testa R; Jakovlevska Z; Efremov G D; Huisman T H
Relative levels of alpha-, beta-, and gamma-mRNA from patients with severe and intermediate beta-thalassemia major.
Acta haematologica 1997;97(4):205-10.
1996: Kazanetz E G; Leonova J Y; Huisman T H; van der Dijs F P; Smit J W
Hb Nunobiki or alpha 2 141 (HC3)Arg-->Cys beta 2 in a Belgian female results from a CGT-->TGT mutation in the alpha 2-globin gene.
Hemoglobin 1996;20(4):443-5.
1996: Dimovski A J; Baysal E; Efremov D G; Prior J F; Raven J L; Efremov G D; Huisman T H
A large beta-thalassemia deletion in a family of Indonesian-Malay descent.
Hemoglobin 1996;20(4):377-92.
1996: Leonova JYe; Kazanetz E G; Smetanina N S; Adekile A D; Efremov G D; Huisman T H
Variability in the fetal hemoglobin level of the normal adult.
American journal of hematology 1996;53(2):59-65.
1996: Carver M F; Huisman T H
International Hemoglobin Information Center variant list.
Hemoglobin 1996;20(3):213.
1996: Smetanina N S; Gu L H; Rodriguez Romero W E; Howard E F; Huisman T H
The relative levels of different types of beta-mRNA and beta-globin in BFU-E derived colonies from patients with beta chain variants; further evidence for somatic mosaicism in the Hb Costa Rica carrier [beta 77(EF1)His-->Arg]
Hemoglobin 1996;20(3):199-212.
1996: Smetanina N S; Oner C; Baysal E; Oner R; Bozkurt G; Altay C; Gürgey A; Adekile A D; Gu L H; Huisman T H
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.
Biochimica et biophysica acta 1996;1316(3):176-82.
1996: Smetanina N S; Huisman T H
MRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants.
American journal of hematology 1996;52(4):258-63.
1996: Rodriguez Romero W E; Castillo M; Chaves M A; Saenz G F; Gu L H; Wilson J B; Baysal E; Smetanina N S; Leonova J Y; Huisman T H
Hb Costa Rica or alpha 2 beta 2 77(EF1)His --> Arg: the first example of a somatic cell mutation in a globin gene.
Human genetics 1996;97(6):829-33.
1996: Adekile A D; Kazanetz E G; Leonova J Y; Marouf R; Khmis A; Huisman T H
Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A).
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1996;18(2):151-3.
1996: Miller D R; Smetanina N S; Gu L H; Leonova J Y; Huisman T H
Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosity.
Hemoglobin 1996;20(2):131-4.
1996: Smetanina N S; Leonova J Y; Levy N; Huisman T H
The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia.
Biochimica et biophysica acta 1996;1315(3):188-92.
1996: Molchanova T P; Huisman T H
The importance of the 3' untranslated region for the expression of the alpha-globin genes.
Hemoglobin 1996;20(1):41-54.
1996: Smetanina N S; Adekile A D; Huisman T H
Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin.
Acta haematologica 1996;96(3):162-9.
1996: Abels J; Michiels J J; Giordano P C; Bernini L F; Baysal E; Smetanina N S; Kazanetz E G; Leonova J Y; Huisman T H
A de novo deletion causing epsilon gamma delta beta-thalassemia in a Dutch patient.
Acta haematologica 1996;96(2):108-9.
1995: Pande P L; Prakash S; Tiwary R S; Kazanetz E G; Leonova J Y e; Huisman T H
Beta-thalassemia intermedia in an Indian female with the Hb Hofu [beta 126(H4)Val-->Glu]-beta zero-thalassemia [codons 8/9 (+G)] combination.
Hemoglobin 1995;19(5):301-6.
1995: Gu L H; Leonova J Y e; Huisman T H
Hb S-Hb Lufkin disease in a black male infant.
Hemoglobin 1995;19(5):291-4.
1995: Gray G R; Manson H E; Gu L H; Leonova JYe; Huisman T H
Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermedia.
American journal of hematology 1995;50(1):26-9.
1995: Molchanova T P; Smetanina N S; Huisman T H
A second, elongated, alpha 2-globin mRNA is present in reticulocytes from normal persons and subjects with terminating codon or poly A mutations.
Biochemical and biophysical research communications 1995;214(3):1184-90.
1995: Cürük M A; Howard S C; Kutlar A; Huisman T H
A newly discovered beta O-thalassemia (IVS-II-850, G-->A) mutation in a north European family.
Hemoglobin 1995;19(3-4):207-11.
1995: Harthoorn-Lasthuizen E J; Nabben F A; Kazanetz E G; Gu L H; Molchanova T P; Huisman T H
HB Mizuho or alpha 2 beta 2 68(E12)Leu-->Pro in a young Dutch boy.
Hemoglobin 1995;19(3-4):203-6.
1995: Gürgey A; Altay C; Gu L H; Leonova J Y; Delibalta A; Oner C; Huisman T H
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow.
Hemoglobin 1995;19(3-4):165-72.
1995: Prchal J T; Adler B; Wilson J B; Baysal E; Qin W B; Molchanova T P; Pobedimskaya D D; Kazanetz E G; Huisman T H
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama.
Hemoglobin 1995;19(3-4):151-64.
1995: Baysal E; Kleanthous M; Bozkurt G; Kyrri A; Kalogirou E; Angastiniotis M; Ioannou P; Huisman T H
alpha-Thalassaemia in the population of Cyprus.
British journal of haematology 1995;89(3):496-9.
1995: Kazanetz E G; Leonova J Y; Wilson J B; McMillan S K; Walbrecht M; de Pablos Gallego J M; Huisman T H
Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNA.
Hemoglobin 1995;19(1-2):1-6.
1995: Gu L H; Oner C; Huisman T H
The G gamma T chain (G gamma 75 Thr; 136 Gly) in Hb F-Charlotte is the product of an A gamma gene with a limited gene conversion and that in Hb F-Waynesboro of a mutated G gamma gene.
Hemoglobin 1995;19(6):413-8.
1995: de Pablos Gallego J M; Gu L H; Leonova JYe; Huisman T H
Hb F-Veleta or alpha 2 G gamma(2)40(C6)Arg-->Gly.
Hemoglobin 1995;19(6):407-11.
1995: Smetanina N S; Gu L H; Leonova JYe; Huisman T H
Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique.
Acta haematologica 1995;93(2-4):105-7.
1995: Smetanina N S; Leonova J Y; Levy N; Huisman T H
Identification of several alpha-globin gene variations in a small Laotian family.
Acta haematologica 1995;94(3):144-7.
1994: Adekile A D; Yüregir T Z; Walker E L; Gu L H; Baysal E; Huisman T H
Factors associated with hypochromia and microcytosis among high school students in the southeastern United States.
Southern medical journal 1994;87(11):1132-7.
1994: Pobedimskaya D D; Molchanova T P; Streichman S; Huisman T H
Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.
American journal of hematology 1994;47(3):198-202.
1994: Molchanova T P; Pobedimskaya D D; Huisman T H
The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
British journal of haematology 1994;88(2):300-6.
1994: Efremov D G; Dimovski A J; Sukarova E; Schilirò G; Zisovski N; Efremov G D; Burrone O R; Huisman T H
gamma-mRNA and Hb F levels in beta-thalassaemia.
British journal of haematology 1994;88(2):311-7.
1994: Pobedimskaya D D; Molchanova T P; Huisman T H
Hb Ramona or alpha (2)24(B5)Tyr-->Cys beta 2.
Hemoglobin 1994;18(4-5):365-6.
1994: Qin W B; Pobedimskaya D D; Molchanova T P; Wilson J B; Gu L H; de Pablos J M; Huisman T H
Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp).
Hemoglobin 1994;18(4-5):297-306.
1994: Baysal E; Huisman T H
Detection of common deletional alpha-thalassemia-2 determinants by PCR.
American journal of hematology 1994;46(3):208-13.
1994: Dimovski A J; Efremov D G; Gu L H; Huisman T H
The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations.
British journal of haematology 1994;87(2):353-6.
1994: Efremov D G; Dimovski A J; Huisman T H
The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin.
Blood 1994;83(11):3350-5.
1994: Bozkurt G; Baysal E; Gu L H; Huisman T H
Thalassemia intermedia in two patients with Hb Lepore-beta zero-thalassemia (Frameshift codon 8, -AA).
Hemoglobin 1994;18(3):247-50.
1994: Baysal E; Sharma S; Wong S C; Jogessar V B; Huisman T H
Distribution of beta-thalassemia mutations in three Asian Indian populations with distant geographical locations.
Hemoglobin 1994;18(3):201-9.
1994: Molchanova T P; Pobedimskaya D D; Ye Z; Huisman T H
Two different mutations in codon 68 are observed in Hb G-Philadelphia heterozygotes.
American journal of hematology 1994;45(4):345-6.
1994: Dimovski A J; Adekile A D; Huisman T H
The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes.
Experientia 1994;50(2):167-70.
1994: Boletini E; Svobodova M; Divoky V; Baysal E; Cürük M A; Dimovski A J; Liang R; Adekile A D; Huisman T H
Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.
Human genetics 1994;93(2):182-7.
1994: Liang R; Liang S; Jiang N H; Wen X J; Zhao J B; Nechtman J F; Stoming T A; Huisman T H
Alpha and beta thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization.
British journal of haematology 1994;86(2):351-4.
1994: Dimovski A J; Divoky V; Adekile A D; Baysal E; Wilson J B; Prior J F; Raven J L; Huisman T H
A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero-thalassemia or hereditary persistence of fetal hemoglobin?
Blood 1994;83(3):822-7.
1994: Divoky V; Baysal E; Oner R; Cürük M A; Walker E L; Indrak K; Huisman T H
The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed.
Human genetics 1994;93(1):77-8.
1994: Qin W B; Baysal E; Wong K F; Molchanova T P; Pobedimskaya D D; Sharma S; Wilson J B; Huisman T H
Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia trait.
American journal of hematology 1994;45(1):91-3.
1994: Dimovski A J; Adekile A D; Divoky V; Baysal E; Huisman T H
Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations.
American journal of hematology 1994;45(1):51-7.
1994: Baysal E; Ribeiro M L; Huisman T H
Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation.
Acta haematologica 1994;91(1):16-20.
1994: Adekile A D; Gu L H; Baysal E; Haider M Z; al-Fuzae L; Aboobacker K C; al-Rashied A; Huisman T H
Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
Acta haematologica 1994;92(4):176-81.
1993: Cürük M A; Dimovski A J; Baysal E; Gu L H; Kutlar F; Molchanova T P; Webber B B; Altay C; Gürgey A; Huisman T H
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
American journal of hematology 1993;44(4):270-5.
1993: Pobedimskaya D D; Molchanova T P; Huisman T H; Harding S R; Bakanec R
Hb F-Saskatoon or alpha 2G gamma (2)21(B3)Glu-->Lys observed in a North American Indian newborn.
Hemoglobin 1993;17(6):547-9.
1993: Pobedimskaya D D; Molchanova T P; Amernick R; Druskin M S; Webber B B; Wilson J B; Huisman T H
Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography.
Hemoglobin 1993;17(6):505-12.
1993: Adekile A D; Dimovski A J; Oner C; Lanclos K D; Huisman T H
Haplotype-specific sequence variations in the locus control region (5' hypersensitive sites 2, 3, 4) of beta S chromosomes.
Hemoglobin 1993;17(5):475-8.
1993: Postnikov YuV; Molchanova T P; Huisman T H
Allele-specific amplification for the identification of several hemoglobin variants.
Hemoglobin 1993;17(5):439-52.
1993: Ringelhann B; Szelenyi J G; Horanyi M; Svobodova M; Divoky V; Indrak K; Hollân S; Marosi A; Laub M; Huisman T H
Molecular characterization of beta-thalassemia in Hungary.
Human genetics 1993;92(4):385-7.
1993: Kutlar F; Huisman T H
New ultra-micro high-performance liquid chromatographic method for determining the gamma chain composition of hemoglobin F in normal adults.
Journal of chromatography 1993;620(2):183-9.
1993: Cürük M A; Baysal E; Gupta R B; Sharma S; Huisman T H
An IVS-I-117 (G-->A) acceptor splice site mutation in the alpha 1-globin gene is a nondeletional alpha-thalassaemia-2 determinant in an Indian population.
British journal of haematology 1993;85(1):148-52.
1993: Gu L H; Wilson J B; Molchanova T P; McKie K M; McKie V C; Huisman T H
Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications.
Hemoglobin 1993;17(4):295-301.
1993: Huisman T H; Gu L H; Liu J C; Fei Y J; Walker E L
Black alpha-thalassemia-1: partial characterization of an approximately 80 kb deletion which includes the zeta- and alpha-globin genes.
Hemoglobin 1993;17(4):345-53.
1993: Divoky V; Svobodova M; Indrak K; Chrobak L; Molchanova T P; Huisman T H
Hb Hradec Kralove (Hb HK) or alpha 2 beta 2 115(G17)Ala-->Asp, a severely unstable hemoglobin variant resulting in a dominant beta-thalassemia trait in a Czech family.
Hemoglobin 1993;17(4):319-28.
1993: Wilson J B; Brennan S O; Allen J; Shaw J G; Gu L H; Huisman T H
The M gamma chain of human fetal hemoglobin is an A gamma chain with an in vitro modification of gamma 141 leucine to hydroxyleucine.
Journal of chromatography 1993;617(1):37-42.
1993: Indrak K; Gu Y C; Novotny J; Huisman T H
A new alpha-thalassemia-2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote.
American journal of hematology 1993;43(2):144-5.
1993: Molchanova T P; Postnikov YuV; Wilson J B; Webber B B; Gu L H; Sabio H; Waldron P; Huisman T H
Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager.
Hemoglobin 1993;17(3):251-4.
1993: Molchanova T P; Postnikov YuV; Gu L H; Prior J F; Raven J L; Bennett J A; Huisman T H
Hb Tigraye or alpha 2 beta (2)79(EF3)Asp-->His(GAC-->CAC): a hemoglobin variant with increased oxygen affinity observed in an Ethiopian male.
Hemoglobin 1993;17(3):247-50.
1993: Molchanova T P; Postnikov YuV; Pobedimskaya D D; Smetanina N S; Moschan A A; Kazanetz E G; Tokarev YuN; Huisman T H
Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNA.
Hemoglobin 1993;17(3):217-25.
1993: Pobedimskaya D D; Molchanova T P; Gu L H; Molina M A; de Pablos J M; Huisman T H
Hb F-Sacromonte or alpha 2G gamma (2)59(E3)Lys-->Gln observed in a Spanish newborn and his mother.
Hemoglobin 1993;17(3):269-74.
1993: Ribeiro M L; Gu L H; Buchanan-Adair I; Huisman T H
Incorrect genetic counseling of a couple with beta-thalassemia, due to incomplete testing.
American journal of human genetics 1993;52(4):842-3.
1993: Divoky V; Gu L H; Indrak K; Mocikova K; Zarnovicanova M; Huisman T H
A new beta zero-thalassaemia nonsense mutation (codon 112, T-->A) not associated with a dominant type of thalassaemia in the heterozygote.
British journal of haematology 1993;83(3):523-4.
1993: Huisman T H
The structure and function of normal and abnormal haemoglobins.
Baillière's clinical haematology 1993;6(1):1-30.
1993: Adekile A D; Liu J C; Sulzer A J; Huisman T H
Frequency of the alpha-thalassemia-2 gene among Nigerian SS patients and its influence on malaria antibody titers.
Hemoglobin 1993;17(1):73-9.
1993: Kutlar F; Kutlar A; Nuguid E; Prchal J; Huisman T H
Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.
Hemoglobin 1993;17(1):55-66.
1993: Tamagnini G P; Gonçalves P; Ribeiro M L; Kaeda J; Kutlar F; Baysal E; Huisman T H
Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations.
Hemoglobin 1993;17(1):31-40.
1993: Divoky V; Baysal E; Schiliro G; Dibenedetto S P; Huisman T H
A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family.
American journal of hematology 1993;42(2):225-6.
1993: Adekile A D; Huisman T H
Hb F in sickle cell anemia.
Experientia 1993;49(1):16-27.
1993: Adekile A D; Huisman T H
Level of fetal hemoglobin in children with sickle cell anemia: influence of gender, haplotype and alpha-thalassemia-2 trait.
Acta haematologica 1993;90(1):34-8.
1992: Cürük M A; Yüregir G T; Asadov C D; Dadasova T; Gu L H; Baysal E; Gu Y C; Ribeiro M L; Huisman T H
Molecular characterization of beta-thalassemia in Azerbaijan.
Human genetics 1992;90(4):417-9.
1992: Divoky V; Bissé E; Wilson J B; Gu L H; Wieland H; Heinrichs I; Prior J F; Huisman T H
Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.
Biochimica et biophysica acta 1992;1180(2):173-9.
1992: Beris P; Kitundu M N; Baysal E; Oner C; Lanclos K D; Dimovski A J; Kutlar F; Huisman T H
Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.
American journal of hematology 1992;41(2):97-101.
1992: Cepreganova B; Wilson J B; Webber B B; Kjovkareska B; Efremov G D; Huisman T H
Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).
Biochemical genetics 1992;30(7-8):385-99.
1992: Adekile A D; Kitundu M N; Gu L H; Lanclos K D; Adeodu O O; Huisman T H
Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.
Annals of hematology 1992;65(1):41-5.
1992: Ribeiro M L; Baysal E; Kutlar F; Tamagnini G P; Gonçalves P; Lopes D; Huisman T H
A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central Portugal.
British journal of haematology 1992;80(4):567-8.
1992: Yüregir G T; Aksoy K; Cürük M A; Dikmen N; Fei Y J; Baysal E; Huisman T H
Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation.
British journal of haematology 1992;80(4):527-32.
1992: Fei Y J; Liu J C; Walker E L; Huisman T H
A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease.
American journal of hematology 1992;39(4):299-300.
1992: Oner C; Dimovski A J; Altay C; Gurgey A; Gu Y C; Huisman T H; Lanclos K D
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes.
Blood 1992;79(3):813-9.
1992: Cepreganova B; Wilson J B; Huisman T H; Hume H A
Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child.
Hemoglobin 1992;16(1-2):77-9.
1992: Cunningham T A; Baker F; Kobrinsky N L; Cepreganova B; Baysal E; Wilson J B; Huisman T H
The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA.
Hemoglobin 1992;16(1-2):19-25.
1992: Fei Y J; Liu J C; Jogessar V B; Westermeyer K R; Bridgemohan R; Huisman T H
Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.
Acta haematologica 1992;87(1-2):11-5.
1992: Molchanova T P; Wilson J B; Gu L H; Guemira F; Fattoum S; Huisman T H
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from Tunisia.
Hemoglobin 1992;16(4):267-73.
1992: Ramachandran M; Gu L H; Wilson J B; Kitundu M N; Adekile A D; Liu J C; McKie K M; Huisman T H
A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family.
Hemoglobin 1992;16(4):259-66.
1992: Huisman T H
The beta- and delta-thalassemia repository.
Hemoglobin 1992;16(4):237-58.
1992: Salkie M L; Higgins T; Morrison D M; Wilson J B; Gu L H; Cürük M A; Baysal E; Huisman T H
A Canadian family with Hb Wayne; characterization by HPLC and DNA sequencing.
Hemoglobin 1992;16(6):515-9.
1992: Liu J S; Molchanova T P; Gu L H; Wilson J B; Hopmeier P; Schnedl W; Balaun E; Krejs G J; Huisman T H
Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria.
Hemoglobin 1992;16(6):493-501.
1992: Webber B B; Wilson J B; Gu L H; Huisman T H
Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2.
Hemoglobin 1992;16(5):441-3.
1992: Fei Y J; Liu J C; McKie V C; Huisman T H
Hb H disease and mild mental retardation in a black girl with a Hb S heterozygosity.
Hemoglobin 1992;16(5):431-4.
1992: Cürük M A; Kutlar A; Huisman T H
Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing.
Hemoglobin 1992;16(5):417-9.
1992: Molchanova T P; Wilson J B; Gu L H; Hain R D; Chang L S; Poon A O; Huisman T H
A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr.
Hemoglobin 1992;16(5):389-98.
1992: Fei Y J; Oner R; Bözkurt G; Gu L H; Altay C; Gurgey A; Fattoum S; Baysal E; Huisman T H
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
Acta haematologica 1992;88(2-3):82-5.
1991: Oner R; Oner C; Wilson J B; Tamagnini G P; Ribeiro L M; Huisman T H
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene.
British journal of haematology 1991;79(2):306-10.
1991: Gonzalez-Redondo J M; Kutlar A; Kutlar F; McKie V C; McKie K M; Baysal E; Huisman T H
Molecular characterization of Hb S(C) beta-thalassemia in American blacks.
American journal of hematology 1991;38(1):9-14.
1991: Jankovic L; Dimovski A J; Kollia P; Karageorga M; Loukopoulos D; Huisman T H
A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia.
International journal of hematology 1991;54(4):289-93.
1991: Indrak K; Indrakova J; Kutlar F; Pospisilova D; Sulovska I; Baysal E; Huisman T H
Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.
Annals of hematology 1991;63(2):111-5.
1991: Kutlar F; Moscoso H; Kiefer C R; Garver F A; Beksaç S; Onderoglu L; Gurgey A; Altay C; Huisman T H
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.
Journal of chromatography 1991;567(2):359-68.
1991: Indrak K; Fei Y J; Li H W; Baysal E; Brabec V; Fortova H; Cermak J; Huisman T H
A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication.
Annals of hematology 1991;63(1):42-4.
1991: Lanclos K D; Oner C; Dimovski A J; Gu Y C; Huisman T H
Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes.
Blood 1991;77(11):2488-96.
1991: Kutlar F; Felice A E; Grech J L; Bannister W H; Kutlar A; Wilson J B; Webber B B; Hu H Y; Huisman T H
The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population.
Human genetics 1991;86(6):591-4.
1991: Plaseska D; Dimovski A J; Wilson J B; Webber B B; Hume H A; Huisman T H
Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location.
Blood 1991;77(1):178-81.
1991: Li H W; Codrington J F; Schiliro G; Wadsworth L D; Beris P; Adekile A; Huisman T H
The usefulness of sequence analysis of amplified DNA for the identification of delta chain variants.
Hemoglobin 1991;15(1-2):77-84.
1991: Indrak K; Brabec V; Wilson J B; Webber B B; Huisman T H
Hb Köln or alpha 2 beta 2(98)(FG5)Val----Met in a Czechoslovakian family.
Hemoglobin 1991;15(1-2):133-5.
1991: Fattoum S; Guemira F; Oner C; Oner R; Li H W; Kutlar F; Huisman T H
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
Hemoglobin 1991;15(1-2):11-21.
1991: Tamagnini G P; Ribeiro M L; Valente V; Ramachandran M; Wilson J B; Baysal E; Gu L H; Huisman T H
Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant.
Hemoglobin 1991;15(6):487-96.
1991: Gupta R B; Tiwary R S; Pande P L; Kutlar F; Oner C; Oner R; Huisman T H
Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
Hemoglobin 1991;15(5):441-58.
1991: Huisman T H; Kutlar F; Gu L H
Gamma chain abnormalities and gamma-globin gene rearrangements in newborn babies of various populations.
Hemoglobin 1991;15(5):349-79.
1991: Altay C; Gurgey A; Oner R; Kutlar A; Kutlar F; Huisman T H
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin 1991;15(4):327-30.
1991: Gu Y C; Gu L H; Wilson J B; Cepreganova B; Ramachandran M; Walker E L; Huisman T H; Potitong P
Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family.
Hemoglobin 1991;15(4):297-302.
1991: Wilson J B; Ramachandran M; Webber B B; Kutlar F; Hazelwood L F; Barnett D; Hirschler N V; Huisman T H
Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----Gln.
Hemoglobin 1991;15(4):269-78.
1991: Cepreganova B; Gu L H; Wilson J B; Huisman T H
A second observation of Hb F-Lodz or alpha 2G gamma (2)44(CD3)Ser----Arg.
Hemoglobin 1991;15(6):549-51.
1991: Keeling M M; Bertolone S J; Baysal E; Gu Y C; Cepreganova B; Wilson J B; Huisman T H
Hb Mizuho or alpha 2 beta (2)68(E12)Leu----Pro in a Caucasian boy with high levels of Hb F; identification by sequencing of amplified DNA.
Hemoglobin 1991;15(6):477-85.
1991: Oner R; Agarwal S; Dimovski A J; Efremov G D; Petkov G H; Altay C; Gurgey A; Huisman T H
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
Hemoglobin 1991;15(1-2):67-76.
1991: Dimovski A J; Oner C; Agarwal S; Gu Y C; Gu L H; Kutlar F; Lanclos K D; Huisman T H
Certain mutations observed in the 5' sequences of the G gamma- and A gamma-globin genes of beta S chromosomes are specific for chromosomes with major haplotypes.
Acta haematologica 1991;85(2):79-87.
1990: Costa F F; Zago M A; Cheng G; Nechtman J F; Stoming T A; Huisman T H
The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C----G substitution at nucleotide -195 of the A gamma-globin gene.
Blood 1990;76(9):1896-7.
1990: Huisman T H
Silent beta-thalassemia and thalassemia intermedia.
Haematologica 1990;75 Suppl 5():1-8.
1990: Codrington J F; Li H W; Kutlar F; Gu L H; Ramachandran M; Huisman T H
Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant.
Blood 1990;76(6):1246-9.
1990: Huisman T H
Frequencies of common beta-thalassaemia alleles among different populations: variability in clinical severity.
British journal of haematology 1990;75(4):454-7.
1990: Kutlar A; Ozcan O; Brisco J T; Ansley M C; Huisman T H
The detection of hemoglobin variants by isoelectrofocusing using EDTA-collected and filter paper-dried cord blood specimens.
American journal of clinical pathology 1990;94(2):199-202.
1990: Oner C; Gurgey A; Altay C; Kutlar F; Huisman T H
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.
American journal of hematology 1990;34(3):230-1.
1990: Efremov G D; Josifovska O; Nikolov N; Codrington J F; Oner C; Gonzalez-Redondo J M; Huisman T H
Hb Icaria-Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA.
British journal of haematology 1990;75(2):250-3.
1990: Kutlar A; Kutlar F; Gu L G; Mayson S M; Huisman T H
Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes.
Human genetics 1990;85(1):106-10.
1990: Jankovic L; Efremov G D; Petkov G; Kattamis C; George E; Yang K G; Stoming T A; Huisman T H
Two novel polyadenylation mutations leading to beta(+)-thalassemia.
British journal of haematology 1990;75(1):122-6.
1990: Kattamis C; Hu H; Cheng G; Reese A L; Gonzalez-Redondo J M; Kutlar A; Kutlar F; Huisman T H
Molecular characterization of beta-thalassaemia in 174 Greek patients with thalassaemia major.
British journal of haematology 1990;74(3):342-6.
1990: Huisman T H
Beta-thalassemia in four Mediterranean countries; an editorial commentary.
Hemoglobin 1990;14(1):35-9.
1990: Zhao W; Wilson J B; Webber B B; Huisman T H; Sciarratta G V; Ivaldi G; Ripamonti M
A second observation of Hb Abruzzo [alpha 2 beta 2(143)(H21)His----Arg] in an Italian family.
Hemoglobin 1990;14(4):463-6.
1990: Zhao W; Wilson J B; Huisman T H; Sciarratta G V; Ivaldi G; Petrini C; Ripamonti M
Hb Camperdown or alpha 2 beta 2(104)(G6)Arg----Ser in two Italian males.
Hemoglobin 1990;14(4):459-61.
1990: Plaseska D; de Alarcon P A; McMillan S; Walbrecht M; Wilson J B; Huisman T H
Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----Ala.
Hemoglobin 1990;14(4):423-9.
1990: Jankovic L; Efremov G D; Josifovska O; Juricic D; Stoming T A; Kutlar A; Huisman T H
An initiation codon mutation as a cause of a beta-thalassemia.
Hemoglobin 1990;14(2):169-76.
1990: Oner R; Altay C; Gurgey A; Aksoy M; Kilinç Y; Stoming T A; Reese A L; Kutlar A; Kutlar F; Huisman T H
Beta-thalassemia in Turkey.
Hemoglobin 1990;14(1):1-13.
1990: Codrington J; Anijs J; Wisse J H; Codrington F A; Li H W; Kutlar F; Ramachandran M; Huisman T H
Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia allele.
Acta haematologica 1990;84(3):135-8.
1990: Huisman T H
Beta-thalassemia repository.
Hemoglobin 1990;14(6):661-75.
1990: Zhao W; Wilson J B; Huisman T H
Low quantities of Hb Boyle Heights or alpha 2(6)(A4)Asp----O beta 2 observed in three members of a Caucasian family.
Hemoglobin 1990;14(6):637-40.
1990: Wilson J B; Webber B B; Plaseska D; de Alarcon P A; McMillan S K; Huisman T H
Hb Davenport or alpha 2(78)(EF7)Asn----His beta 2.
Hemoglobin 1990;14(6):599-605.
1990: Plaseska D; Wilson J B; Gu L H; Kutlar F; Huisman T H; Zeng Y T; Shen M
Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met.
Hemoglobin 1990;14(5):555-7.
1990: Plaseska D; Gu L H; Wilson J B; Codrington J F; Huisman T H; Dash S
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult.
Hemoglobin 1990;14(5):491-7.
1990: Harkness M; Harkness D R; Kutlar F; Kutlar A; Wilson J B; Webber B B; Codrington J F; Huisman T H
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities.
Hemoglobin 1990;14(5):479-89.
1990: Zhao W; Wilson J B; Webber B B; Kutlar A; Tamagnini G P; Kuam B; Huisman T H
Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.
Hemoglobin 1990;14(6):627-35.
1990: Plaseska D; Kutlar F; Wilson J B; Fei Y J; Huisman T H
Hb F-Charlotte, an A gamma variant with a threonine residue in position gamma 75 and a glycine residue in position gamma 136.
Hemoglobin 1990;14(6):617-25.
1990: Plaseska D; Wilson J B; Kutlar F; Font L; Baiget M; Huisman T H
Hb F-Catalonia or alpha 2G gamma(2)15(A12)Trp----Arg.
Hemoglobin 1990;14(5):511-6.
1990: Agarwal S; Oner R; Kutlar F; Huisman T H
Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes.
Hemoglobin 1990;14(4):471-5.
1990: Plaseska D; Li H J; Wilson J B; Kutlar F; Kutlar A; Huisman T H; Kulpa J
Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.
Hemoglobin 1990;14(2):213-6.
1990: Plaseska D; Kutlar F; Wilson J B; Webber B B; Zeng Y T; Huisman T H
Hb F-Jiangsu, the first gamma chain variant with a valine----methionine substitution: alpha 2A gamma 2 134(H12)Val----Met.
Hemoglobin 1990;14(2):177-83.
1989: Mishima N; Landman H; Huisman T H; Gilman J G
The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence.
British journal of haematology 1989;73(3):375-9.
1989: Bhaumik K; Huisman T H
Application of high-performance liquid chromatographic methodology to the analysis of hemoglobins synthesized in erythroid progenitor cells.
Journal of chromatography 1989;496(1):83-9.
1989: Codrington J F; Kutlar F; Harris H F; Wilson J B; Stoming T A; Huisman T H
Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA.
Biochimica et biophysica acta 1989;1009(1):87-9.
1989: Ojwang P J; Ogada T; Gonzalez-Redondo J M; Kutlar A; Kutlar F; Huisman T H
beta S-haplotypes and alpha-thalassemia along the coastal belt of Kenya.
East African medical journal 1989;66(6):377-80.
1989: Lanclos K D; Michael S K; Gu Y C; Howard E F; Stoming T A; Huisman T H
Transient chloramphenicol acetyltransferase expression of the G gamma globin gene 5'-flanking regions containing substitutions of C----T at position -158, G----A at position -161, and T----A at position -175 in K562 cells.
Biochimica et biophysica acta 1989;1008(1):109-12.
1989: Yang K G; Kutlar F; George E; Wilson J B; Kutlar A; Stoming T A; Gonzalez-Redondo J M; Huisman T H
Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.
British journal of haematology 1989;72(1):73-80.
1989: Huisman T H
Usefulness of cation exchange high performance liquid chromatography as a testing procedure.
Pediatrics 1989;83(5 Pt 2):849-51.
1989: Kutlar F; Gonzalez-Redondo J M; Kutlar A; Gurgey A; Altay C; Efremov G D; Kleman K; Huisman T H
The levels of zeta, gamma, and delta chains in patients with Hb H disease.
Human genetics 1989;82(2):179-86.
1989: Han I S; Huang H J; Zeng Y T; Lanclos K D; Huisman T H
Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes.
Blood 1989;73(3):845-8.
1989: Kutlar F; Gu L H; Hu H; Huisman T H
Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography.
Journal of chromatography 1989;487(2):265-74.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar F; Kutlar A; McKie V C; McKie K M; Huisman T H
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.
British journal of haematology 1989;71(1):113-7.
1989: Stoming T A; Stoming G S; Lanclos K D; Fei Y J; Altay C; Kutlar F; Huisman T H
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.
Blood 1989;73(1):329-33.
1989: Gonzalez-Redondo J M; Kattamis C; Huisman T H
Characterization of three types of beta zero-thalassemia resulting from a partial deletion of the beta-globin gene.
Hemoglobin 1989;13(4):377-92.
1989: Prior J F; Raven J L; Wilson J B; Kutlar A; Kutlar F; Huisman T H
Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family.
Hemoglobin 1989;13(1):79-81.
1989: Wong S C; Stoming T A; Efremov G D; Huisman T H
High frequencies of a rearrangement (+ATA; -T) at -530 to the beta-globin gene in different populations indicate the absence of a correlation with a silent beta-thalassemia determinant.
Hemoglobin 1989;13(1):1-5.
1989: Huisman T H
Beta-thalassemia repository.
Hemoglobin 1989;13(7-8):775-87.
1989: Kutlar F; Reese A L; Hsia Y E; Kleman K M; Huisman T H
The types of hemoglobins and globin chains in hydrops fetalis.
Hemoglobin 1989;13(7-8):671-83.
1989: Kollia P; Gonzalez-Redondo J M; Stoming T A; Loukopoulos D; Politis C; Huisman T H
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.
Hemoglobin 1989;13(6):597-604.
1989: Wilson J B; Webber B B; Kutlar A; Reese A L; McKie V C; Lutcher C L; Felice A E; Huisman T H
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.
Hemoglobin 1989;13(6):557-66.
1989: Codrington J F; Codrington F A; Wisse J H; Wilson J B; Webber B B; Wong S C; Huisman T H
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S.
Hemoglobin 1989;13(6):543-56.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar F; Kutlar A; Hu H; Wilson J B; Huisman T H
Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron.
Hemoglobin 1989;13(1):67-74.
1989: Gurgey A; Altay C; Beksaç M S; Bhattacharya R; Kutlar F; Huisman T H
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
Acta haematologica 1989;81(3):169-71.
1989: Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.
Hemoglobin 1989;13(6):623-4.
1989: Kutlar A; Kutlar F; Aksoy M; Gurgey A; Altay C; Wilson J B; Diaz-Chico J C; Hu H; Huisman T H
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
Hemoglobin 1989;13(1):7-16.
1989: Gurgey A; Altay C; Diaz-Chico J C; Kutlar F; Kutlar A; Huisman T H
Molecular heterogeneity of beta-thalassemia intermedia in Turkey.
Acta haematologica 1989;81(1):22-7.
1988: Gonzalez-Redondo J M; Diaz-Chico J C; Malcorra-Azpiazu J J; Balda-Aguirre M I; Huisman T H
Characterization of a newly discovered alpha-thalassaemia-1 in two Spanish patients with Hb H disease.
British journal of haematology 1988;70(4):459-63.
1988: Gilman J G; Mishima N; Wen X J; Stoming T A; Lobel J; Huisman T H
Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin.
Nucleic acids research 1988;16(22):10635-42.
1988: Gonzalez-Redondo J M; Kutlar F; Kutlar A; Stoming T A; de Pablos J M; Kilinç Y; Huisman T H
Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A.
British journal of haematology 1988;70(1):85-9.
1988: Fei Y J; Lanclos K D; Kutlar F; Walker E L; Huisman T H
A chromosome with five gamma-globin genes.
Blood 1988;72(2):827-9.
1988: Liu J Z; Gilman J G; Cao Q; Bakioglu I; Huisman T H
Four categories of gamma-globin gene triplications: DNA sequence comparison of low G gamma and high G gamma triplications.
Blood 1988;72(2):480-4.
1988: Gilman J G; Mishima N; Wen X J; Kutlar F; Huisman T H
Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults.
Blood 1988;72(1):78-81.
1988: Fei Y J; Stoming T A; Efremov G D; Efremov D G; Battacharia R; Gonzalez-Redondo J M; Altay C; Gurgey A; Huisman T H
Beta-thalassemia due to a T----A mutation within the ATA box.
Biochemical and biophysical research communications 1988;153(2):741-7.
1988: Gu Y C; Nakatsuji T; Huisman T H
Detection of a new hybrid alpha 2 globin gene among American blacks.
Human genetics 1988;79(1):68-72.
1988: Yang K G; Stoming T A; Fei Y J; Liang S; Wong S C; Masala B; Huang R B; Wei Z P; Huisman T H
Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.
Blood 1988;71(5):1414-7.
1988: Gonzalez-Redondo J M; Han I S; Gu Y C; Huisman T H
Nucleotide sequence of the human theta 1-globin gene.
Biochemical genetics 1988;26(3-4):207-11.
1988: Aluoch J R; Hamming H D; Nijenhuis N E; Bakioglu I; Huisman T H
Homozygous beta+-thalassemia in a Dutch teenager: haematological, clinical, and genetic observations. A case report.
The Netherlands journal of medicine 1988;32(3-4):130-5.
1988: Efremov D G; Efremov G D; Zisovski N; Stojanovski N; Kutlar F; Diaz-Chico J C; Kutlar A; Yang K G; Stoming T A; Huisman T H
Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia.
British journal of haematology 1988;68(3):351-5.
1988: Fei Y J; Fujita S; Huisman T H
Two different theta (theta) globin gene deletions observed among black newborn babies.
British journal of haematology 1988;68(2):249-53.
1988: Diaz-Chico J C; Yang K G; Yang K Y; Efremov D G; Stoming T A; Huisman T H
The detection of beta-globin gene mutations in beta-thalassemia using oligonucleotide probes and amplified DNA.
Biochimica et biophysica acta 1988;949(1):43-8.
1988: Malcorra-Azpiazu J J; Balda-Aguirre M I; Diaz-Chico J C; Kutlar F; Kutlar A; Wilson J B; Hu H; Huisman T H
Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family.
Hemoglobin 1988;12(2):201-5.
1988: Malcorra-Azpiazu J J; Balda-Aguirre M I; Diaz-Chico J C; Hu H; Wilson J B; Webber B B; Kutlar F; Kutlar A; Huisman T H
Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant.
Hemoglobin 1988;12(2):163-70.
1988: Liu J Z; Huisman T H
Construction of three plasmids, each containing two or three different human globin gene fragments.
Hemoglobin 1988;12(5-6):755-61.
1988: Liang S; Tang Z N; Su Z W; Long G F; Liang R; Huisman T H; Fei Y J
The thalassemia syndromes in association with hemoglobinopathies in southern China.
Hemoglobin 1988;12(5-6):579.
1988: Stoming T A; Diaz-Chico J C; Yang K G; Efremov D G; Huisman T H
Newer developments in the identification of beta-thalassemia.
Hemoglobin 1988;12(5-6):565-76.
1988: Diaz-Chico J C; Huang H J; Juricic D; Efremov G D; Wadsworth L D; Huisman T H
Two new large deletions resulting in epsilon gamma delta beta-thalassemia.
Acta haematologica 1988;80(2):79-84.
1988: Huisman T H; Fei Y J; Kutlar F
Variations in G gamma and A gamma ratios in the fetal hemoglobin of newborn babies.
Hemoglobin 1988;12(5-6):699-705.
1988: Kutlar A; Kutlar F; Wilson J B; Webber B B; Hu H; Huisman T H
Hb F-Austell or alpha 2G gamma (2)40(C6)Arg----Lys.
Hemoglobin 1988;12(4):409-11.
1988: Altay C; Gurgey A; Wilson J B; Hu H; Webber B B; Kutlar F; Huisman T H
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.
Hemoglobin 1988;12(1):87-9.
1987: Efremov G D; Gjorgovski I; Stojanovski N; Diaz-Chico J C; Harano T; Kutlar F; Huisman T H
One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.
Human genetics 1987;77(2):132-6.
1987: Lanclos K D; Patterson J; Efremov G D; Wong S C; Villegas A; Ojwang P J; Wilson J B; Kutlar F; Huisman T H
Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya.
Human genetics 1987;77(1):40-5.
1987: Huang H J; Stoming T A; Harris H F; Kutlar F; Huisman T H
The Greek A gamma beta+-HPFH observed in a large black family.
American journal of hematology 1987;25(4):401-8.
1987: Diaz-Chico J C; Yang K G; Kutlar A; Reese A L; Aksoy M; Huisman T H
An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta-thalassemia.
Blood 1987;70(2):583-6.
1987: Ojwang P J; Ogada T; Beris P; Hattori Y; Lanclos K D; Kutlar A; Kutlar F; Huisman T H
Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from Kenya.
British journal of haematology 1987;65(2):211-5.
1987: Altay C; Kutlar A; Wilson J B; Webber B B; Huisman T H
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family.
Hemoglobin 1987;11(4):395-9.
1987: Indrak K; Wiedermann B F; Batek F; Wilson J B; Webber B B; Kutlar A; Huisman T H
Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant.
Hemoglobin 1987;11(2):151-5.
1987: Efremov G D; Jankovic L; Juricic D; Stojancov A; Wilson J B; Webber B B; Kutlar F; Kutlar A; Hu H; Huisman T H
Hb Bushwick [beta 74(E18)Gly----Val] heterozygotes in a Yugoslavian family have 35 to 40% of the unstable variant.
Hemoglobin 1987;11(6):557-62.
1987: Huisman T H
High-performance liquid chromatography as a method to identify haemoglobin abnormalities.
Acta haematologica 1987;78(2-3):123-6.
1987: Kutlar F; Kutlar A; Gu Y C; Huisman T H
Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies.
Acta haematologica 1987;78(1):28-32.
1987: Huisman T H; Kutlar F; Kutlar A; Wilson J B; Harris H F
The M gamma chain of human fetal hemoglobin.
Progress in clinical and biological research 1987;251():507-17.
1987: Gilman J G; Kutlar F; Johnson M E; Huisman T H
A G to A nucleotide substitution 161 base pairs 5' of the G gamma globin gene cap site (-161) in a high G gamma non-anemic person.
Progress in clinical and biological research 1987;251():383-90.
1987: Huisman T H
A short review of human gamma-globin gene anomalies.
Acta haematologica 1987;78(2-3):80-4.
1986: Efremov G D; Nikolov N; Hattori Y; Bakioglu I; Huisman T H
The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes.
Blood 1986;68(4):971-4.
1986: Aluoch J R; Kilinç Y; Aksoy M; Yüregir G T; Bakioglu I; Kutlar A; Kutlar F; Huisman T H
Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observations.
British journal of haematology 1986;64(1):45-55.
1986: Felice A E; Cleek M P; Marino E M; McKie K M; McKie V C; Chang B K; Huisman T H
Different zeta globin gene deletions among black Americans.
Human genetics 1986;73(3):221-4.
1986: Aksoy M; Gurgey A; Altay C; Kilinc Y; Carstairs K C; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Some notes about Hb Q-India and Hb Q-Iran.
Hemoglobin 1986;10(2):215-9.
1986: Hsu L; Lung Q F; Tang Z N; Fei Y J; Su C W; Chen S S; Webber B B; Wilson J B; Kutlar F; Huisman T H
Hb Chapel Hill or alpha 274(EF3)Asp----Gly beta 2 observed in a Chinese family in association with beta-thalassemia.
Hemoglobin 1986;10(1):77-86.
1986: Wiedermann B F; Indrak K; Wilson J B; Webber B B; Yang K G; Kutlar F; Kutlar A; Huisman T H
Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male.
Hemoglobin 1986;10(6):673-6.
1986: Lanclos K D; Kutlar A; Kutlar F; Ojwang P J; Reese A L; Huisman T H
The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes.
Hemoglobin 1986;10(4):401-16.
1985: Aksoy M; Kutlar A; Efremov G D; Nikolov N; Petkov G; Reese A L; Harano T; Chen S S; Huisman T H
Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.
American journal of hematology 1985;20(1):7-16.
1985: Henthorn P S; Smithies O; Nakatsuji T; Felice A E; Gardiner M B; Reese A L; Huisman T H
(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA.
British journal of haematology 1985;59(2):343-56.
1985: Juricic D; Efremov G D; Wilson J B; Huisman T H
Hb Savaria or alpha(2)49(CE7)Ser----Arg beta 2 in a Yugoslavian family.
Hemoglobin 1985;9(6):631-3.
1985: Carstairs K C; Raulfs A; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada.
Hemoglobin 1985;9(2):201-5.
1985: Ojwang P J; Ogada T; Webber B B; Wilson J B; Huisman T H
Hb Savaria or alpha2 (49)(CE7)Ser----Arg beta2 in an indigenous female from Kenya.
Hemoglobin 1985;9(2):197-200.
1985: Kilinç Y; Kumi M; Gurgey A; Altay C; Webber B B; Wilson J B; Kutlar A; Huisman T H
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
Hemoglobin 1985;9(6):621-5.
1985: Gilman J G; Harano T; Nakatsuji T; Bakioglu I; Reese A L; Gardiner M B; Huisman T H
The ratio of the G gamma and A gamma chains: variations due to anomalies at the molecular level.
Annals of the New York Academy of Sciences 1985;445():235-47.
1984: Ojwang P J; Ogada T; Bakioglu I; Headlee M G; Reese A L; Huisman T H
Abnormal human haemoglobins in western Kenya.
East African medical journal 1984;61(12):886-91.
1984: Nakatsuji T; Gilman J G; Sukumaran P K; Huisman T H
Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFH.
British journal of haematology 1984;57(4):663-70.
1984: Bakioglu I; Reese A L; Huisman T H
A comparison of two procedures useful for the isolation of Hb F from adult red blood cells and for the quantitation of the types of gamma chain by high-performance liquid chromatography.
Journal of chromatography 1984;295(1):171-7.
1984: Felice A E; Cleek M P; McKie K; McKie V; Huisman T H
The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.
Blood 1984;63(5):1253-7.
1984: Kutlar A; Gardiner M B; Headlee M G; Reese A L; Cleek M P; Nagle S; Sukumaran P K; Huisman T H
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain.
Biochemical genetics 1984;22(1-2):21-35.
1984: Sciarratta G V; Ivaldi G; Molaro G L; Sansone G; Salkie M L; Wilson J B; Reese A L; Huisman T H
The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.
Hemoglobin 1984;8(2):169-81.
1984: Nakatsuji T; Headlee M G; Huisman T H
Hemoglobin Kariya or alpha 240(C5)Lys----Glu beta 2 in a Caucasian family from South Carolina.
Hemoglobin 1984;8(4):401-5.
1984: Huisman T H; Headlee M G; Wilson J B; Lam H; Johnson S E; Webber B B
Hb Wayne, the frameshift variant with extended alpha chains observed in a Caucasian family from Alabama.
Hemoglobin 1984;8(1):1-15.
1984: Gilman J G; Huisman T H; Stojanovski N; Efremov G D
Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient.
Hemoglobin 1984;8(5):529-34.
1983: Cleek M P; Gardiner M B; Reese A L; Harris H F; Felice A E; Huisman T H
The Atlanta family with hemoglobin Grady revisited.
American journal of human genetics 1983;35(6):1314-6.
1983: Zeng Y T; Huang S Z; Reynolds A; Lam H; Webber B B; Wilson J B; Huisman T H
Application of high pressure liquid chromatography and microsequencing methodology in the structural analysis of human hemoglobin variants.
Scientia Sinica. Series B, Chemical, biological, agricultural, medical & earth sciences / Chung-kuo k'o hsüeh yüan, chu pan 1983;26(8):836-49.
1983: Sukumaran P K; Nakatsuji T; Gardiner M B; Reese A L; Gilman J G; Huisman T H
Gamma thalassemia resulting from the deletion of a gamma-globin gene.
Nucleic acids research 1983;11(13):4635-43.
1983: Headlee M E; Gardiner M B; Reese A L; Huisman T H
The distribution of fetal hemoglobin and the types of gamma chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies.
Biochemical medicine 1983;29(3):337-54.
1983: Huisman T H; Reese A L; Gardiner M B; Wilson J B; Lam H; Reynolds A; Nagle S; Trowell P; Zeng Y T; Huang S Z; Sukumaran P K; Miwa S; Efremov G D; Petkov G; Sciarratta G V; Sansone G
The occurrence of different levels of G gamma chain and of the A gamma T variant of fetal hemoglobin in newborn babies from several countries.
American journal of hematology 1983;14(2):133-48.
1983: Nakatsuji T; Carver J; Wilson J B; Lam H; Reese A L; Nagle S; Miwa S; Huisman T H
alpha Chain and gamma chain abnormal hemoglobins in newborn babies: structural and genetic aspects.
American journal of hematology 1983;14(2):121-32.
1983: Headlee M G; Nakatsuji T; Lam H; Wrightstone R N; Huisman T H
Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent.
Hemoglobin 1983;7(3):285-7.
1983: Cin S; Akar N; Cavdar A O; Arcasoy A; Dedeoglu S; Webber B; Lam H; Huisman T H
Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus.
Hemoglobin 1983;7(5):467-70.
1983: Juricic D; Crepinko I; Efremov G D; Lam H; Webber B B; Headlee M G; Huisman T H
Hb A2-Zagreb or alpha 2 delta 2(125)(H3)Gln replaced by Glu, a new delta chain variant in association with delta beta-thalassemia.
Hemoglobin 1983;7(5):443-8.
1983: Romero Garcia C; Navarro J L; Lam H; Webber B B; Headlee M G; Wilson J B; Huisman T H
Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family.
Hemoglobin 1983;7(5):435-42.
1983: Ojwang P J; Nakatsuji T; Gardiner M B; Reese A L; Gilman J G; Huisman T H
Gene deletion as the molecular basis for the Kenya-G gamma-HPFH condition.
Hemoglobin 1983;7(2):115-23.
1982: Yi-Tao Z; Headlee M E; Henson J; Lam H; Wilson J B; Huisman T H
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.
Biochimica et biophysica acta 1982;707(2):206-12.
1982: Gardiner M B; Reese A L; Headlee M E; Huisman T H
The heterogeneity of the gamma-chain of fetal hemoglobin in HbS heterozygotes.
Blood 1982;60(2):513-8.
1982: Efremov G D; Ibarra B; Gurgey A; Sukumaran P K; Altay C; Huisman T H
Gamma-chain heterogeneity of fetal hemoglobin in nonblack beta- and delta beta- thalassemia and HPFH heterozygotes and homozygotes.
American journal of hematology 1982;12(4):367-82.
1982: Fuhr J E; Bamberger E; Lozzio C B; Lozzio B B; Felice A E; Altay G; Webber B B; Reese A L; Mayson S M; Huisman T H
Identification and quantitation of embryonic and three types of fetal hemoglobin produced on induction of the human pluripotent leukemia cell line K-562 with hemin.
American journal of hematology 1982;12(1):1-12.
1982: Salkie M L; Gordon P A; Rigal W M; Lam H; Wilson J B; Headlee M E; Huisman T H
Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia.
Hemoglobin 1982;6(3):223-31.
1982: Zeng Y T; Huang S Z; Yen Y K; Li W C; Lam H; Webber B; Wilson J B; Huisman T H
Hemoglobin Queens (alpha 34 (B15) Leu replaced by Arg) found in two Chinese families.
Hemoglobin 1982;6(2):209-11.
1982: Sciarratta G V; Sansone G; Valbonesi M; Wilson J B; Lam H; Webber B B; Headlee M E; Huisman T H
Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian male.
Hemoglobin 1982;6(4):419-21.
1982: Nakatsuji T; Headlee M; Lam H; Wilson J B; Huisman T H
Hb F-Bonaire-Ga or alpha 2 A gamma 2 39(C5) Gln replaced by Arg, characterized by high pressure liquid chromatographic and microsequencing procedures.
Hemoglobin 1982;6(6):599-606.
1982: Nakatsuji T; Lam H; Carver J; Huisman T H
Hb F-Marietta or G gamma I 80[EF4] Asp replaced by Asn, observed in a Caucasian baby.
Hemoglobin 1982;6(4):407-11.
1982: Nakatsuji T; Webber B; Lam H; Wilson J B; Huisman T H; Sciarratta G V; Sansone G; Molaro G L
A new gamma chain variant: Hb F-Pordenone [gamma 6(A3) Glu replaced by Gln: 75ILE: 136ALA].
Hemoglobin 1982;6(4):397-401.
1982: Reese A L; Altay C; Headlee M E; Gardiner M B; Webber B; Jonah F; Wilson J B; Huisman T H
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemia.
Hemoglobin 1982;6(4):369-78.
1981: Huisman T H; Gravely M E; Webber B; Okonjo K; Henson J; Reese A L
The gamma chain heterogeneity of fetal hemoglobin in black beta-thalassemia and HPFH heterozygotes.
Blood 1981;58(1):62-70.
1981: Huisman T H; Altay C; Webber B; Reese A L; Gravely M E; Okonjo K; Wilson J B
Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition.
Blood 1981;57(1):75-82.
1981: Prozorova-Zamani V; Ozsoylu S; Aksoy M; Headlee M G; Lam H; Wilson J B; Altay C; Huisman T H
Hb E and Hb E-like variants in individuals from Turkey.
Hemoglobin 1981;5(7-8):743-8.
1981: Efremov G D; Markovska B; Stojanovski N; Petkov G; Nikolov N; Huisman T H
The use of globin chain electrophoresis in polyacrylamide gels for the quantitation of the G gamma to A gamma ratio in fetal hemoglobin.
Hemoglobin 1981;5(7-8):637-51.
1981: Huisman T H; Webber B; Okonjo K; Reese A L; Wilson J B
The separation of human hemoglobin chains by high pressure liquid chromatography.
Progress in clinical and biological research 1981;60():23-38.
1981: Huisman T H; Reese A L; Webber B; Okonjo K; Altay C; Felice A E
In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies form person with alpha- or beta-thalassemia.
American journal of hematology 1981;10(3):227-37.
1980: Alter B P; Goff S C; Efremov G D; Gravely M E; Huisman T H
Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis.
British journal of haematology 1980;44(4):527-34.
1980: Felice A E; Mayson S M; Webber B B; Miller A; Gravely M E; Huisman T H
Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family.
Pediatric research 1980;14(3):266-7.
1980: Huisman T H; Abraham B L; Harris H F; Gravely M E; Henson J; Williams D; Wilson J B; Miller A; Mayson S; Wrightstone R N; Moss E; Joseph B; Walker L; Brisco J; Brisco L
Hemoglobinopathies observed in the population of the Southeastern United States (SE-USA).
Hemoglobin 1980;4(3-4):373-86.
1980: Huisman T H; Reese A L; Gravely M E; Harris H; Wilson J B
The synthesis of the G gamma and A gamma chains of human fetal hemoglobin in erythroid colonies cultured from peripheral blood BFUe's of normal adults and newborn and of subjects with an A gamma or a G gamma chain abnormal fetal hemoglobin.
American journal of hematology 1980;9(2):137-50.
1980: Huisman T H; Reese A L; Gravely M E; Wilson J B; Webber B; Felice A E
Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH).
Hemoglobin 1980;4(3-4):449-67.
1980: Huisman T H; Efremov G D; Reese A L; Howard J S; Gravely M E; Wilson J B
The ratio of G gamma and A gamma chains of the hemoglobin F synthesized by BFU-E-derived colonies from blood of subjects with beta+ thalassemia and related hemoglobinopathies.
Annals of the New York Academy of Sciences 1980;344():253-61.

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