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Ferdane Kutlar

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Kutlar F; Hilliard L M; Zhuang L; Patel N; Eroglu B; Meiler S E; Carmichael H; Russell R B; Kutlar A
Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.
Hughes Heather Yaun; McKie Kathleen; Carmichael Harris; Bora Komal; Kutlar Abdullah; Kutlar Ferdane
Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
Subbannan Karthi; Ustun Celalettin; Natarajan Kavita; Clair Betsy; Daitch Lisa; Fields Sabine; Kutlar Ferdane; Kutlar Abdullah
Acute splenic complications and implications of splenectomy in hemoglobin SC disease.

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All Publications

2009: Kutlar F; Hilliard L M; Zhuang L; Patel N; Eroglu B; Meiler S E; Carmichael H; Russell R B; Kutlar A
Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.
Blood cells, molecules & diseases 2009;43(3):235-8.
2009: Hughes Heather Yaun; McKie Kathleen; Carmichael Harris; Bora Komal; Kutlar Abdullah; Kutlar Ferdane
Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
Annals of hematology 2009;88(11):1151-3.
2009: Subbannan Karthi; Ustun Celalettin; Natarajan Kavita; Clair Betsy; Daitch Lisa; Fields Sabine; Kutlar Ferdane; Kutlar Abdullah
Acute splenic complications and implications of splenectomy in hemoglobin SC disease.
European journal of haematology 2009;83(3):258-60.
2009: McKeown Sean M; Carmichael Harris; Markowitz Rhea-Beth; Kutlar Abdullah; Holley Leslie; Kutlar Ferdane
Rare occurrence of Hb Lepore-Baltimore in African Americans: molecular characteristics and variations of Hb Lepores.
Annals of hematology 2009;88(6):545-8.
2009: Akl Pascale S; Kutlar Ferdane; Patel Niren; Salisbury Catherine L; Lane Peter; Young Andrew N
Compound heterozygosity for hemoglobin S [beta6(A3)Glu6Val] and hemoglobin Korle-Bu [beta73(E17)Asp73Asn].
Laboratory hematology : official publication of the International Society for Laboratory Hematology 2009;15(3):20-4.
2008: Perry Rodney T; Gearhart Debra A; Wiener Howard W; Harrell Lindy E; Barton James C; Kutlar Abdullah; Kutlar Ferdane; Ozcan Ozan; Go Rodney C P; Hill William D
Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease.
Neurobiology of aging 2008;29(2):185-93.
2008: Dainer Erin; Shell Richard; Miller Randy; Atkin Joan F; Pastore Matt; Kutlar Abdullah; Zhuang Lina; Holley Leslie; Davis Debra H; Kutlar Ferdane
Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT].
Hemoglobin 2008;32(6):596-600.
2008: Dainer Erin; Wenk Robert E; Luddy Ruth; Elam Dedrey; Holley Leslie; Kutlar Abdullah; Kutlar Ferdane
Two new hemoglobin variants: Hb Sinai-Greenspring [beta34(B16)Val-->Ile, GTC > ATC] and Hb Sinai-Bel Air [beta53(D4)Ala-->Asp, GCT > GAT].
Hemoglobin 2008;32(6):588-91.
2007: Agarwal Neeraj; Kutlar Ferdane; Mojica-Henshaw Mariluz P; Ou Ching N; Gaikwad Amos; Reading N Scott; Bailey Lakeia; Kutlar Abdullah; Prchal Josef T
Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele.
Haematologica 2007;92(12):1715-6.
2007: Steiner Laurie A; Van Hoff Jack; Kutlar Ferdane; Gallagher Patrick G
Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review.
Hemoglobin 2007;31(4):409-16.
2007: Kutlar Ferdane
Diagnostic approach to hemoglobinopathies.
Hemoglobin 2007;31(2):243-50.
2006: Dinçol Gunçag; Güvenç Serkan; Elam Dedrey; Kutlar Abdullah; Kutlar Ferdane
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish male.
International journal of medical sciences 2006;3(1):26-7.
2005: Adekile A; Kutlar F; McKie K; Addington A; Elam D; Holley L; Clair B; Kutlar A
The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
European journal of haematology 2005;75(2):150-5.
2005: Kutlar F; Mirmow D; Glendenning M; Holley L; Kutlar A
Postmortem molecular diagnosis of sickle beta thalassaemia.
Journal of clinical pathology 2005;58(5):548-9.
2005: Adekile Adekunle; Haider Mohammad; Kutlar Ferdane
Mutations associated with beta-thalassemia intermedia in Kuwait.
Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2005;14 Suppl 1():69-72.
2004: Vinson Amy E; Walker Aisha; Elam Dedrey; Glendenning Michele; Kutlar Ferdane; Clair Betsy; Harbin Jeanette; Kutlar Abdullah
A novel approach to rapid determination of betaS-globin haplotypes: sequencing of the Agamma-IVS-II region.
Hemoglobin 2004;28(4):317-23.
2003: Dinçol Gunçag; Elam Dedrey; Kutlar Abdullah; Kutlar Ferdane
Hb Setif [alpha94(G1)Asp --> Tyr (alpha2)] detected in a Turkish family.
Hemoglobin 2003;27(4):249-52.
2003: Adams Gaye T; Snieder Harold; McKie Virgil C; Clair Betsy; Brambilla Donald; Adams Robert J; Kutlar Ferdane; Kutlar Abdullah
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen.
BMC medical genetics 2003;4():6.
2003: Ustun Celatettin; Kutlar Ferdane; Holley Leslie; Seigler Maree; Burgess Russell; Kutlar Abdullah
Interaction of sickle cell trait with hereditary spherocytosis: splenic infarcts and sequestration.
Acta haematologica 2003;109(1):46-9.
2002: Redding-Lallinger Rupa; Tankut Gaye; Holley Leslie; Wright Frances; Kutlar Abdullah; Kutlar Ferdane
Molecular characterization of Hb D-Ibadan [beta87(F3)Thr-->Lys] in combination with Hb S [beta6(A3)Glu-->Val] and with beta+-Thalassemia: report of two cases.
Hemoglobin 2002;26(2):129-34.
2001: Kutlar A; Kutlar F; Turker I; Tural C
The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease.
Hemoglobin 2001;25(2):213-7.
2001: Adekile A D; Kutlar F; Haider M Z; Kutlar A
Frequency of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients.
American journal of hematology 2001;66(4):263-6.
2000: Aguinaga M D; Kutlar F; Turner E A; Park D
Hb Inkster [alpha85(F6)Asp-->Val] found in a caucasian male with polycythemia.
Hemoglobin 2000;24(4):333-9.
1999: Tadmouri G O; Bilenoglu O; Kutlar F; Markowitz R B; Kutlar A; Basak A N
Identification of the Chinese IVS-II-654 (C-->T) beta-thalassemia mutation in an immigrant Turkish family: recurrence or migration?
Human biology; an international record of research 1999;71(2):295-302.
1998: Long Q; Bengra C; Li C; Kutlar F; Tuan D
A long terminal repeat of the human endogenous retrovirus ERV-9 is located in the 5' boundary area of the human beta-globin locus control region.
Genomics 1998;54(3):542-55.
1998: Tuohy A M; McKie V C; Sabio H; Kutlar F; Kutlar A; Wilson J B
Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1998;20(6):563-6.
1998: Kutlar F; Adamkiewicz T V; Markowitz R B; Holley L; Kutlar A
An alpha-2 globin gene initiation codon mutation in a Vietnamese patient with Hb H disease.
Annals of the New York Academy of Sciences 1998;850():398-400.
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: 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: Adekile A D; McKie K M; Adeodu O O; Sulzer A J; Liu J S; McKie V C; Kutlar F; Ramachandran M; Kaine W; Akenzua G I
Spleen in sickle cell anemia: comparative studies of Nigerian and U.S. patients.
American journal of hematology 1993;42(3):316-21.
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.
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: 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: Indrak K; Brabec V; Indrakova J; Chrobak L; Sakalova A; Jarosova M; Cermak J; Fei Y J; Kutlar F; Gu Y C
Molecular characterization of beta-thalassemia in Czechoslovakia.
Human genetics 1992;88(4):399-404.
1991: Niazi G A; Yaish H M; Kutlar F; Huisman T H
Heterogeneity of gamma-globin chain synthesis in Saudi newborns.
International journal of hematology 1991;54(5):377-83.
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: 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: 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: Oner R; Kutlar F; Gu L H; Huisman T H
The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene.
Blood 1991;77(5):1124-5.
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: 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: 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: 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: 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: 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: 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: Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Codrington J F; Prchal J T; Hall K M; de Pablos J M; Rodriguez I
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.
Blood 1990;75(9):1883-7.
1990: Petkov G H; Efremov G D; Efremov D G; Dimovski A; Tchaicarova P; Tchaicarov R; Rogina B; Agarwal S; Kutlar A; Kutlar F
Beta-thalassemia in Bulgaria.
Hemoglobin 1990;14(1):25-33.
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: 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: 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: 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: Harano T; Harano K; Doi K; Ueda S; Imai K; Ohba Y; Kutlar F; Huisman T H
Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.
Hemoglobin 1990;14(2):217-22.
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: 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: 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: Gonzalez-Redondo J M; Stoming T A; Kutlar A; Kutlar F; Lanclos K D; Howard E F; Fei Y J; Aksoy M; Altay C; Gurgey A
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
Blood 1989;73(6):1705-11.
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: 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: Bird A R; Elliott T; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time.
Hemoglobin 1989;13(2):193-7.
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: Fei Y J; Kutlar F; Harris H F; Wilson M M; Milana A; Sciacca P; Schiliro G; Masala B; Manca L; Altay C
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns.
Hemoglobin 1989;13(1):45-65.
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: Ulukutlu L; Ozsahin H; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl.
Hemoglobin 1989;13(5):509-13.
1989: Villegas A; Martín G; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Hb Extremadura or alpha 2 beta 2133 (H11)Val----Leu, a new mildly unstable hemoglobin in a Spanish female.
Hemoglobin 1989;13(5):505-8.
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: Glader B E; Zwerdling D; Kutlar F; Kutlar A; Wilson J B; Huisman T H
Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.
Hemoglobin 1989;13(7-8):769-73.
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; 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: Gonzalez-Redondo J M; Stoming T A; Lanclos K D; Gu Y C; Kutlar A; Kutlar F; Nakatsuji T; Deng B; Han I S; McKie V C
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
Blood 1988;72(3):1007-14.
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: 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: 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: Diaz-Chico J C; Yang K G; Stoming T A; Efremov D G; Kutlar A; Kutlar F; Aksoy M; Altay C; Gurgey A; Kilinc Y
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
Blood 1988;71(1):248-51.
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: Ali M A; Pinkerton P; Chow S W; Zaetz S D; Wilson J B; Webber B B; Hu H; Kutlar A; Kutlar F; Huisman T H
Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg]
Hemoglobin 1988;12(2):137-48.
1988: Liang S; Tang Z; Su C; Lung Q; Liang R; Fei Y J; Kutlar F; Wilson J B; Webber B B; Hu H
Hb Duan [alpha 75(EF4)Asp----Ala], Hb Westmead [alpha 122(H5)His----Gln], and alpha-thalassemia-2 (-4.2 Kb deletion) in a Chinese family.
Hemoglobin 1988;12(1):13-21.
1988: Harano T; Harano K; Ukita M; Wada Y; Hayashi A; Ohba Y; Miyaji T; Kutlar F; Huisman T H
Characterization of abnormalities in the gamma-globin gene arrangements of Japanese newborns.
Hemoglobin 1988;12(5-6):723-39.
1988: Masala B; Manca L; Gallisai D; Stangoni A; Lanclos K D; Kutlar F; Yang K G; Huisman T H
Biochemical and molecular aspects of beta-thalassemia types in northern Sardinia.
Hemoglobin 1988;12(5-6):661-71.
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: Kutlar F; Fei Y J; Wilson J B; Kutlar A; Huisman T H
Detection of the embryonic zeta chain in blood from newborn babies by reversed-phase high-performance liquid chromatography.
Journal of chromatography 1987;394(2):333-43.
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: Huisman T H; Kutlar F; Kutlar A; Wilson J B; Harris H F
The M gamma chain of human fetal hemoglobin; its identification and occurrence.
Journal of chromatography 1987;388(2):429-39.
1987: Bird A R; Elliot T E; Wilson J B; Webber B B; Kutlar F; Kutlar A; Huisman T H
Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female.
Hemoglobin 1987;11(2):157-60.
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: 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: de Pablos J M; Wilson J B; Kutlar A; Kutlar F; Webber B B; Huisman T H
Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn.
Hemoglobin 1987;11(5):513-6.
1987: Ma M; Hu H; Kutlar F; Wilson J B; Huisman T H
Hb F-Xin-Su or A gamma I73(E17)Asp----His: a new slow-moving fetal hemoglobin variant.
Hemoglobin 1987;11(5):473-9.
1987: Kutlar A; Kutlar F; Wilson J B; Webber B B; Gonzalez Redondo J M; Huisman T H
Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.
Hemoglobin 1987;11(2):185-8.
1987: Chu Z F; Liang C C; Kutlar F; Huisman T H
Fetal hemoglobin heterogeneity in Chinese newborns of the Uygur and Han nationalities; comparisons of babies from Xinjiang and Beijing.
Hemoglobin 1987;11(2):123-8.
1986: Yang K G; Liu J Z; Kutlar F; Kutlar A; Altay C; Gurgey A; Huisman T H
Beta zero-thalassemia in association with a gamma-globin gene quadruplication.
Blood 1986;68(6):1394-7.
1986: Hattori Y; Kutlar F; Chen S S; Huisman T H; Demuro P; Formato M; Manca L; Masala B
DNA polymorphisms in North Sardinian newborns and their linkage with abnormal gamma globin gene arrangements and with beta (0) -thalassemia.
Biochemical genetics 1986;24(9-10):669-81.
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: Nakatsuji T; Kutlar A; Kutlar F; Huisman T H
Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplication.
American journal of human genetics 1986;38(6):981-3.
1986: Efremov G D; Filipce V; Gjorgovski I; Juricic D; Stojanovski N; Harano T; Nakatsuji T; Kutlar A; Kutlar F; Bakioglu I
G gamma A gamma(delta beta)zero-thalassaemia and a new form of gamma globin gene triplication identified in the Yugoslavian population.
British journal of haematology 1986;63(1):17-28.
1986: Kutlar F; Kutlar A; Huisman T H
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography.
Journal of chromatography 1986;357(1):147-53.
1986: Shimizu K; Harano T; Harano K; Miwa S; Amenomori Y; Ohba Y; Kutlar F; Huisman T H
Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.
American journal of human genetics 1986;38(1):45-58.
1986: Wilson J B; Chen S S; Webber B B; Kutlar A; Kutlar F; Villegas A; Huisman T H
The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic procedures.
Hemoglobin 1986;10(1):49-63.
1986: Bowman J E; Bloom R; Chen S S; Webber B B; Wilson J B; Kutlar F; Kutlar A; Huisman T H
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family.
Hemoglobin 1986;10(5):495-505.
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: Hattori Y; Kutlar F; Kutlar A; McKie V C; Huisman T H
Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia.
Hemoglobin 1986;10(6):623-42.
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.
1986: Hattori Y; Kutlar F; Mosley C J; Mayson S M; Huisman T H
Association of the level of G gamma chain in the fetal hemoglobin of normal adults with specific haplotypes.
Hemoglobin 1986;10(2):185-204.
1985: Harano K; Harano T; Kutlar F; Huisman T H
gamma-Globin gene triplication and quadruplication in Japanese newborns. Evidence for a decreased in vivo expression of the 3'-A gamma-globin gene.
FEBS letters 1985;190(1):45-9.
1985: Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Bastesbihçi S
Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
Journal of medical genetics 1985;22(4):288-90.
1985: Aksoy M; Kutlar A; Kutlar F; Harano T; Chen S S; Huisman T H
Hemoglobin H disease in two Turkish females and one Iranian newborn.
Hemoglobin 1985;9(4):373-84.
1985: Kutlar A; Hattori Y; Bakioglu I; Kutlar F; Kamel K; Huisman T H
Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31.
Hemoglobin 1985;9(6):545-57.
1985: Huisman T H; Chen S S; Nakatsuji T; Kutlar F
A second family with the Atlanta type of HPFH.
Hemoglobin 1985;9(4):393-8.
1985: Huisman T H; Kutlar F; Nakatsuji T; Bruce-Tagoe A; Kilinç Y; Cauchi M N; Romero Garcia C
The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.
Human genetics 1985;71(2):127-33.
1984: Kutlar A; Kutlar F; Wilson J B; Headlee M G; Huisman T H
Quantitation of hemoglobin components by high-performance cation-exchange liquid chromatography: its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants.
American journal of hematology 1984;17(1):39-53.
1984: Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Wilson J B; Huisman T H
Hb Beograd-beta zero thalassemia in a Turkish family from Yugoslavia.
Hemoglobin 1984;8(4):417-21.

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