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David Chui

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
Koenig Sara C; Becirevic Esmira; Hellberg Miriam S C; Li Michael Y; So Jason C C; Hankins Jane S; Ware Russell E; McMahon Lillian; Steinberg Martin H; Luo Hong-Yuan; Chui David H K
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
Moradkhani Kamran; Préhu Claude; Old John; Henderson Shirley; Balamitsa Vera; Luo Hong-Yuan; Poon Man-Chiu; Chui David H K; Wajcman Henri; Patrinos George P
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.
Thornburg Courtney D; Steinberg Martin H; Chui David H K
Hemoglobin SE disease in Maine, and severe thalassemia in New Hampshire.

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All Publications

2009: Koenig Sara C; Becirevic Esmira; Hellberg Miriam S C; Li Michael Y; So Jason C C; Hankins Jane S; Ware Russell E; McMahon Lillian; Steinberg Martin H; Luo Hong-Yuan; Chui David H K
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
American journal of hematology 2009;84(9):603-6.
2009: Moradkhani Kamran; Préhu Claude; Old John; Henderson Shirley; Balamitsa Vera; Luo Hong-Yuan; Poon Man-Chiu; Chui David H K; Wajcman Henri; Patrinos George P
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.
Annals of hematology 2009;88(6):535-43.
2009: Thornburg Courtney D; Steinberg Martin H; Chui David H K
Hemoglobin SE disease in Maine, and severe thalassemia in New Hampshire.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2009;31(4):307.
2009: Chen Zhiyi; Luo Hong-yuan; Steinberg Martin H; Chui David H K
BCL11A represses HBG transcription in K562 cells.
Blood cells, molecules & diseases 2009;42(2):144-9.
2009: Wilcox Ibifiri; Boettger Kevin; Greene Lance; Malek Anita; Davis Lance; Steinberg Martin H; Luo Hong-Yuan; Chui David H K
Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
American journal of hematology 2009;84(1):55-8.
2008: Sedgewick Amanda E; Timofeev Nadia; Sebastiani Paola; So Jason C C; Ma Edmond S K; Chan Li Chong; Fucharoen Goonnapa; Fucharoen Supan; Barbosa Cynara G; Vardarajan Badri N; Farrer Lindsay A; Baldwin Clinton T; Steinberg Martin H; Chui David H K
BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
Blood cells, molecules & diseases 2008;41(3):255-8.
2008: Chen Zhiyi; Luo Hong-Yuan; Basran Raveen K; Hsu Tien-Huei; Mang Daniel W H; Nuntakarn Lalana; Rosenfield Cathy G; Patrinos George P; Hardison Ross C; Steinberg Martin H; Chui David H K
A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.
Molecular and cellular biology 2008;28(13):4386-93.
2008: Gibney Geoffrey T; Panhuysen Carolien I M; So Jason C C; Ma Edmond S K; Ha Shau Yin; Li Chi Kong; Lee Anselm C W; Li Chi Keung; Yuen Hui Leung; Lau Yu Lung; Johnson David M; Farrell John J; Bisbee Alice B; Farrer Lindsay A; Steinberg Martin H; Chan Li Chong; Chui David H K
Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong.
American journal of hematology 2008;83(6):458-64.
2008: Basran Raveen K; Reiss Ulrike M; Luo Hong-Yuan; Ware Russell E; Chui David H K
Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.
Pediatric blood & cancer 2008;50(2):363-6.
2007: Tubman Venée N; Bennett Carolyn M; Luo Hong-yuan; Chui David H K; Heeney Matthew M
Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.
Pediatric blood & cancer 2007;49(2):207-10.
2007: Masiello David; Heeney Matthew M; Adewoye Adeboye H; Eung Shawn H; Luo Hong-Yuan; Steinberg Martin H; Chui David H K
Hemoglobin SE disease: a concise review.
American journal of hematology 2007;82(7):643-9.
2007: Waye J S; Chui D H K
Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
Haematologica 2007;92(5):e68.
2007: Shinoda Gen; Umeda Katsutsugu; Heike Toshio; Arai Masato; Niwa Akira; Ma Feng; Suemori Hirofumi; Luo Hong Yuan; Chui David H K; Torii Ryuzo; Shibuya Masabumi; Nakatsuji Norio; Nakahata Tatsutoshi
alpha4-Integrin(+) endothelium derived from primate embryonic stem cells generates primitive and definitive hematopoietic cells.
Blood 2007;109(6):2406-15.
2007: Giardine Belinda; van Baal Sjozef; Kaimakis Polynikis; Riemer Cathy; Miller Webb; Samara Maria; Kollia Panagoula; Anagnou Nicholas P; Chui David H K; Wajcman Henri; Hardison Ross C; Patrinos George P
HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.
Human mutation 2007;28(2):206.
2007: Andersson B Anders R; Wering Mikaela E L; Luo Hong-Yuan; Basran Raveen K; Steinberg Martin H; Smith Hedy P; Chui David H K
Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
European journal of haematology 2007;78(1):82-5.
2007: Luo Hong-Yuang; Adewoye Adeboye H; Pilichowska Monika; Li Michael Yunlong; Basran Raveen K; Steinberg Martin H; Chui David H K
Two new alpha-thalassemia frameshift mutations.
Hemoglobin 2007;31(2):135-9.
2006: Umeda Katsutsugu; Heike Toshio; Nakata-Hizume Mami; Niwa Akira; Arai Masato; Shinoda Gen; Ma Feng; Suemori Hirofumi; Luo Hong Yuan; Chui David H K; Torii Ryuzo; Shibuya Masabumi; Nakatsuji Norio; Nakahata Tatsutoshi
Sequential analysis of alpha- and beta-globin gene expression during erythropoietic differentiation from primate embryonic stem cells.
Stem cells (Dayton, Ohio) 2006;24(12):2627-36.
2006: Luo Hong-Yuan; Heeney Matthew; Wang Winfred C; Eung Shawn H; Ware Russell E; Steinberg Martin H; Chui David H K
Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
American journal of hematology 2006;81(5):361-5.
2006: Umeda Katsutsugu; Heike Toshio; Yoshimoto Momoko; Shinoda Gen; Shiota Mitsutaka; Suemori Hirofumi; Luo Hong Yuan; Chui David H K; Torii Ryuzo; Shibuya Masabumi; Nakatsuji Norio; Nakahata Tatsutoshi
Identification and characterization of hemoangiogenic progenitors during cynomolgus monkey embryonic stem cell differentiation.
Stem cells (Dayton, Ohio) 2006;24(5):1348-58.
2006: Chan Amy Yuk-Yin; Luo Hong-Yuan; Wang Wen; Chui David H K; Ma Edmond Shiu-Kwan; Chan Li-Chong; Chong Samuel S
Diagnostic pitfall in PCR-based alpha-thalassemia genotyping resulting from a (G->C) polymorphism at nucleotide 71 3' to the alpha2-globin gene termination codon.
Clinical chemistry 2006;52(3):536-7.
2006: Law Hai-Yang; Luo Hong-Yuan; Wang Wen; Ho Julia F V; Najmabadi Hossein; Ng Ivy S L; Steinberg Martin H; Chui David H K; Chong Samuel S
Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.
Haematologica 2006;91(3):297-302.
2006: Chui David H K; Cunningham Melody J; Luo Hong-Yuan; Wolfe Lawrence C; Neufeld Ellis J; Steinberg Martin H
Screening and counseling for thalassemia.
Blood 2006;107(4):1735-7.
2005: Luo H-Y; Tang W; Eung S H; Coad J E; Canfield P; Keller F; Crowell E H; Steinberg M H; Chui D H K
Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG).
Journal of clinical pathology 2005;58(10):1110-2.
2005: Luo Hong-yuan; Boudreaux Jeanne; Steinberg Martin H; Chui David H K
Patients with thalassemia in the United States.
Blood 2005;105(12):4896-7.
2005: Chui David H K
Alpha-thalassaemia and population health in Southeast Asia.
Annals of human biology 2005;32(2):123-30.
2005: Lau Elizabeth T; Kwok Yvonne K; Luo Hong Yuan; Leung K Y; Lee C P; Lam Y H; Chui David H K; Tang Mary H Y
Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.
Prenatal diagnosis 2005;25(2):123-8.
2005: Basran Raveen K; Patterson Margie; Walker Lynda; Nakamura Lisa M; Eng Barry; Chui David H K; Waye John S
Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.
Annals of the New York Academy of Sciences 2005;1054():507-10.
2005: Chui David H K
Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.
Annals of the New York Academy of Sciences 2005;1054():25-32.
2004: Luo Hong-Yuan; Irving Ian; Prior John; Lim Erna; Eung Shawn H; Skelton Timothy P; Erber Wendy N; Steinberg Martin H; Chui David H K
Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.
American journal of hematology 2004;77(4):384-6.
2004: Luo Hong-Yuan; Adewoye Adeboye H; Eung Shawn H; Skelton Timothy P; Quillen Karen; McMahon Lillian; Steinberg Martin H; Chui David H K
A novel sickle hemoglobin: hemoglobin S-south end.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2004;26(11):773-6.
2004: Ding Chunming; Chiu Rossa W K; Lau Tze K; Leung Tse N; Chan Li C; Chan Amy Y Y; Charoenkwan Pimlak; Ng Ivy S L; Law Hai-Yang; Ma Edmond S K; Xu Xiangmin; Wanapirak Chanane; Sanguansermsri Torpong; Liao Can; Ai Mary Anne Tan Jin; Chui David H K; Cantor Charles R; Lo Y M Dennis
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(29):10762-7.
2004: Umeda Katsutsugu; Heike Toshio; Yoshimoto Momoko; Shiota Mitsutaka; Suemori Hirofumi; Luo Hong Yuan; Chui David H K; Torii Ryuzo; Shibuya Masabumi; Nakatsuji Norio; Nakahata Tatsutoshi
Development of primitive and definitive hematopoiesis from nonhuman primate embryonic stem cells in vitro.
Development (Cambridge, England) 2004;131(8):1869-79.
2004: Patrinos George P; Giardine Belinda; Riemer Cathy; Miller Webb; Chui David H K; Anagnou Nicholas P; Wajcman Henri; Hardison Ross C
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.
Nucleic acids research 2004;32(Database issue):D537-41.
2004: Ingle John; Adewoye Adeboye; Dewan Robert; Okoli Michael; Rollins Lamarr; Eung Shawn H; Luo Hong-Yuan; Chui David H K; Steinberg Martin H
Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia.
Hemoglobin 2004;28(4):277-85.
2003: Waye John S; Patterson Margaret; Walker Lynda; Eng Barry; Nakamura Lisa M; Lafferty John D; Yong Siu-Li; Wu John K; Chui David H K;
Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.
American journal of hematology 2003;74(3):179-81.
2003: Wang Wen; Ma Edmond S K; Chan Amy Y Y; Prior John; Erber Wendy N; Chan Li C; Chui David H K; Chong Samuel S
Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 alpha-globin gene triplications.
Clinical chemistry 2003;49(10):1679-82.
2003: Patterson Margie; Walker Lynda; Chui David H K; Cohen Alan R; Waye John S
Identification of a new beta-thalassemia nonsense mutation [codon 59 (AAG-->TAG)].
Hemoglobin 2003;27(3):201-3.
2003: Patterson Margie; Walker Lynda; Chui David H K; Lafferty John D; McFarlane Andrew; Waye John S
Identification of a new hemoglobin variant: Hb St. Joseph's [beta77(EF1)His-->Leu].
Hemoglobin 2003;27(3):181-3.
2003: Wang Wen; Ma Edmond S K; Chan Amy Y Y; Chui David H K; Chong Samuel S
Multiple minisequencing screen for seven southeast Asian nondeletional alpha-thalassemia mutations.
Clinical chemistry 2003;49(5):800-3.
2003: Chui David H K; Fucharoen Suthat; Chan Vivian
Hemoglobin H disease: not necessarily a benign disorder.
Blood 2003;101(3):791-800.
2003: Lafferty John D; Waye John S; Chui David H K; Crawford Linda; Raby Anne; Richardson Harold;
Good practice guidelines for laboratory investigation of hemoglobinopathies.
Laboratory hematology : official publication of the International Society for Laboratory Hematology 2003;9(4):237-45.
2002: Chiu Rossa W K; Lau Tze K; Leung Tse N; Chow Katherine C K; Chui David H K; Lo Y M Dennis
Prenatal exclusion of beta thalassaemia major by examination of maternal plasma.
Lancet 2002;360(9338):998-1000.
2002: Hardison Ross C; Chui David H K; Giardine Belinda; Riemer Cathy; Patrinos George P; Anagnou Nicholas; Miller Webb; Wajcman Henri
HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.
Human mutation 2002;19(3):225-33.
2002: Waye John S; Walker Lynda; Patterson Margaret; Chui David H K
Identification of two new beta-thalassemia splice mutations: IVS-I-1 (G-->C) and IVS-I (-2) (A-->C).
Hemoglobin 2002;26(1):87-9.
2002: Waye John S; Walker Lynda; Lafferty John; Lemire Edmond G; Chui David H K
Dominant beta-thalassemia due to a newly identified frameshift mutation in exon 3 (codon 113, GTG-->Tg).
Hemoglobin 2002;26(1):83-6.
2002: Ma S K; Ma Victor; Chan Amy Y Y; Chan L C; Chui David H K
Routine screening of (--(SEA)) alpha-thalassemia deletion by an enzyme-linked immunosorbent assay for embryonic zeta-globin chains.
Acta haematologica 2002;108(1):8-12.
2001: Lorey F; Charoenkwan P; Witkowska H E; Lafferty J; Patterson M; Eng B; Waye J S; Finklestein J Z; Chui D H
Hb H hydrops foetalis syndrome: a case report and review of literature.
British journal of haematology 2001;115(1):72-8.
2001: Su Y Y; Gordon C T; Ye T Z; Perkins A C; Chui D H
Human ERMAP: an erythroid adhesion/receptor transmembrane protein.
Blood cells, molecules & diseases 2001;27(5):938-49.
2001: Waye J S; Eng B; Patterson M; Walker L; Carcao M D; Olivieri N F; Chui D H
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
American journal of hematology 2001;68(1):11-5.
2001: Lau E T; Kwok Y K; Chui D H; Wong H S; Luo H Y; Tang M H
Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures.
Prenatal diagnosis 2001;21(7):529-39.
2001: Hardison R C; Chui D H; Riemer C; Giardine B; Lehväslaiho H; Wajcman H; Miller W
Databases of human hemoglobin variants and other resources at the globin gene server.
Hemoglobin 2001;25(2):183-93.
2001: Waye J S; Chui D H
The alpha-globin gene cluster: genetics and disorders.
Clinical and investigative medicine. Médecine clinique et experimentale 2001;24(2):103-9.
2001: Chan L C; Ma S K; Chan A Y; Ha S Y; Waye J S; Lau Y L; Chui D H
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
Journal of clinical pathology 2001;54(4):317-20.
2001: Leung K F; Au W Y; Chan A Y; Chan L C; Waye J S; Chui D H; Ma S K
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family.
Clinical and laboratory haematology 2001;23(1):53-5.
2001: Waye J S; Eng B; Patterson M; Reis M D; Macdonald D; Chui D H
Novel beta-thalassemia mutation in a beta-thalassemia intermedia patient.
Hemoglobin 2001;25(1):103-5.
2001: Chui D H; Dover G J
Sickle cell disease: no longer a single gene disorder.
Current opinion in pediatrics 2001;13(1):22-7.
2001: Eng B; Patterson M; Walker L; Chui D H; Waye J S
Detection of severe nondeletional alpha-thalassemia mutations using a single-tube multiplex ARMS assay.
Genetic testing 2001;5(4):327-9.
2001: Lorey F; Cunningham G; Vichinsky E P; Lubin B H; Witkowska H E; Matsunaga A; Azimi M; Sherwin J; Eastman J; Farina F; Waye J S; Chui D H
Universal newborn screening for Hb H disease in California.
Genetic testing 2001;5(2):93-100.
2000: Lafferty J D; Crowther M A; Waye J S; Chui D H
A reliable screening test to identify adult carriers of the (--SEA) alpha zero-thalassemia deletion. Detection of embryonic zeta-globin chains by enzyme-linked immunosorbent assay.
American journal of clinical pathology 2000;114(6):927-31.
2000: Waye J S; Eng B; Chui D H; Powers P J; Lafferty J D
Second report of Hb Toulon [alpha77(EF6)Pro-->His] in a Canadian family of Italian descent.
Hemoglobin 2000;24(4):359-60.
2000: Waye J S; Walker L; Chui D H; Lafferty J; Kirby M
Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H disease.
Hemoglobin 2000;24(4):355-7.
2000: Ma S K; Chow E Y; Chan A Y; Kung N N; Waye J S; Chan L C; Chui D H
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation.
American journal of hematology 2000;64(3):206-9.
2000: Ye T Z; Gordon C T; Lai Y H; Fujiwara Y; Peters L L; Perkins A C; Chui D H
Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein.
Gene 2000;242(1-2):337-45.
2000: Eng B; Patterson M; Borys S; Chui D H; Waye J S
PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletions.
American journal of hematology 2000;63(1):54-6.
1999: Waye J S; Borys S; Eng B; Patterson M; Chui D H; Badr El-Din O M; Aref M K; Afify Z
Spectrum of beta-thalassemia mutations in Egypt.
Hemoglobin 1999;23(3):255-61.
1998: Chui D H; Hardison R; Riemer C; Miller W; Carver M F; Molchanova T P; Efremov G D; Huisman T H
An electronic database of human hemoglobin variants on the World Wide Web.
Blood 1998;91(8):2643-4.
1998: Chui D H; Waye J S
Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.
Blood 1998;91(7):2213-22.
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: 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: Waye J S; Eng B; Patterson M; Chui D H; Fernandes B J
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)].
Hemoglobin 1998;22(1):83-5.
1997: Waye J S; Eng B; Patterson M; Barr R D; Chui D H
De novo mutation of the beta-globin gene initiation codon (ATG-->AAG) in a Northern European boy.
American journal of hematology 1997;56(3):179-82.
1997: Waye J S; Eng B; Patterson M; Chui D H; Nisbet-Brown E; Olivieri N F
Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H disease.
Hemoglobin 1997;21(5):469-72.
1997: Tang W; Lai Y H; Han X D; Wong P M; Peters L L; Chui D H
Murine Hn1 on chromosome 11 is expressed in hemopoietic and brain tissues.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(9):695-6.
1997: Waye J S; Eng B; Patterson M; Chui D H; Fernandes B J
Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T).
Hemoglobin 1997;21(4):385-7.
1997: Lau Y L; Chan L C; Chan Y Y; Ha S Y; Yeung C Y; Waye J S; Chui D H
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screening.
The New England journal of medicine 1997;336(18):1298-301.
1995: Waye J S; Eng B; Patterson M; Wasi P; Chui D H; Francombe W H; Sher G D; Olivieri N F
Severity of beta-thalassemia due to genotypes involving the IVS-I-6 (T-->C) mutation.
American journal of hematology 1995;50(1):15-9.
1995: Luo H Y; Deisseroth A B; Chui D H
Human embryonic zeta-globin gene expression in mouse-human hybrid erythroid cell lines.
Blood 1995;86(3):1212-7.
1995: Chui D H; Tang W; Orkin S H
cDNA cloning of murine Nrf 2 gene, coding for a p45 NF-E2 related transcription factor.
Biochemical and biophysical research communications 1995;209(1):40-6.
1995: Waye J S; Eng B; Francombe W H; Chui D H
Novel seventeen basepair deletion in exon 3 of the beta-globin gene.
Human mutation 1995;6(3):252-3.
1994: Waye J S; Eng B; Patterson M; Chui D H; Chang L S; Cogionis B; Poon A O; Olivieri N F
Hb E/Hb LeporeHollandia in a family from Bangladesh.
American journal of hematology 1994;47(4):262-5.
1994: Waye J S; Eng B; Hunt J A; Chui D H
Filipino beta-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosis.
Human genetics 1994;94(5):530-2.
1994: Waye J S; Eng B; Olivieri N F; Chui D H
Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosis.
Prenatal diagnosis 1994;14(10):929-32.
1994: Waye J S; Patterson M; Eng B; Chui D H; Sher G D; Olivieri N F
DNA diagnosis of Hb S and Hb Caribbean (alpha 2 beta 2 91 Leu-->Arg) in a Jamaican family.
American journal of hematology 1994;47(1):33-5.
1993: Tang W; Luo H Y; Eng B; Waye J S; Chui D H
Immunocytological test to detect adult carriers of (--SEA/) deletional alpha-thalassaemia.
Lancet 1993;342(8880):1145-7.
1993: Waye J S; Eng B; Cai S P; Patterson M; Smith J; Tang W; Chui D H
Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.
Clinical and investigative medicine. Médecine clinique et experimentale 1993;16(5):358-71.
1993: Tang W; Cai S P; Eng B; Poon M C; Waye J S; Illum N; Chui D H
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia.
Blood 1993;81(6):1636-40.
1993: Eng B; Chui D H; Saunderson J; Olivieri N F; Waye J S
Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.
Human mutation 1993;2(5):375-9.
1992: Waye J S; Cai S P; Eng B; Chui D H; Francombe W H
Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin Kenya.
American journal of hematology 1992;41(4):289-91.
1992: Tang W; Luo H Y; Albitar M; Patterson M; Eng B; Waye J S; Liebhaber S A; Higgs D R; Chui D H
Human embryonic zeta-globin chain expression in deletional alpha-thalassemias.
Blood 1992;80(2):517-22.
1992: Waye J S; Eng B; Chui D H
Identification of an extensive zeta-alpha globin gene deletion in a Chinese individual.
British journal of haematology 1992;80(3):378-80.
1992: Cai S P; Eng B; Francombe W H; Olivieri N F; Kendall A G; Waye J S; Chui D H
Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene.
Blood 1992;79(5):1342-6.
1991: Steinberg M H; Coleman M B; Adams J G; Waye J S; Chui D H
High hemoglobin A2 beta-thalassemia.
The Journal of laboratory and clinical medicine 1991;118(4):382.
1991: Cai S P; Eng B; Kan Y W; Chui D H
A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to beta-thalassemia.
Human genetics 1991;87(6):728-30.
1991: Waye J S; Chui D H; Eng B; Cai S P; Coleman M B; Adams J G; Steinberg M H
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.
American journal of hematology 1991;38(2):108-12.
1991: Cai S P; Chui D H; Ng J; Poon A O; Freedman M H; Olivieri N F
A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family.
American journal of hematology 1991;37(1):6-8.
1991: Waye J S; Cai S P; Eng B; Clark C; Adams J G; Chui D H; Steinberg M H
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.
Blood 1991;77(5):1100-3.
1990: Chui D H; Patterson M; Dowling C E; Kazazian H H; Kendall A G
Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.
The New England journal of medicine 1990;323(3):179-82.
1989: Toles J F; Chui D H; Belbeck L W; Starr E; Barker J E
Hemopoietic stem cells in murine embryonic yolk sac and peripheral blood.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(19):7456-9.
1989: Chui D H; Mentzer W C; Patterson M; Iarocci T A; Embury S H; Perrine S P; Mibashan R S; Higgs D R
Human embryonic zeta-globin chains in fetal and newborn blood.
Blood 1989;74(4):1409-14.
1988: Luo H Y; Clarke B J; Gauldie J; Patterson M; Liao S K; Chui D H
A novel monoclonal antibody based diagnostic test for alpha-thalassemia-1 carriers due to the (-SEA/) deletion.
Blood 1988;72(5):1589-94.
1988: Devraj-Kizuk R; Chui D H; Prochownik E V; Carter C J; Ofosu F A; Blajchman M A
Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity.
Blood 1988;72(5):1518-23.
1988: Zhao J Q; Luo H Y; Clarke B J; Chui D H
An immunoassay to detect human embryonic epsilon globin chains by a murine monoclonal antibody.
Blood 1988;71(4):883-7.
1988: Chui D H; Luo H Y; Clarke B J
Potential application of a new screening test for alpha-thalassemia-1 carriers.
Hemoglobin 1988;12(5-6):459-63.
1987: Bowman E; Watts J; Burrows R; Chui D H
Hemoglobin barts hydrops fetalis syndrome.
Haematologia 1987;20(3):125-30.
1986: Wong P M; Chung S W; Chui D H; Eaves C J
Properties of the earliest clonogenic hemopoietic precursors to appear in the developing murine yolk sac.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(11):3851-4.
1986: Wong P M; Chung S W; Reicheld S M; Chui D H
Hemoglobin switching during murine embryonic development: evidence for two populations of embryonic erythropoietic progenitor cells.
Blood 1986;67(3):716-21.
1985: Wong P M; Chung S W; Eaves C J; Chui D H
Ontogeny of the mouse hemopoietic system.
Progress in clinical and biological research 1985;193():17-28.
1984: Chung S W; Wong S C; Clarke B J; Patterson M; Walker W H; Chui D H
Human embryonic zeta-globin chains in adult patients with alpha-thalassemias.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(19):6188-91.
1983: Wong P M; Chung S W; White J S; Reicheld S M; Patterson M; Clarke B J; Chui D H
Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cells.
Blood 1983;62(6):1280-8.
1983: Harvey A R; Clarke B J; Chui D H; Kean W F; Buchanan W W
Anemia associated with rheumatoid disease. Inverse correlation between erythropoiesis and both IgM and rheumatoid factor levels.
Arthritis and rheumatism 1983;26(1):28-34.
1982: Clarke B J; Brickenden A M; Ives R A; Chui D H
Effect of modulators of erythropoiesis on the hemoglobinization of human erythroid cell cultures.
Blood 1982;60(2):346-51.
1982: Chui D H; Clarke B J
Abnormal erythroid progenitor cells in human preleukemia.
Blood 1982;60(2):362-7.
1982: Wong P M; Clarke B J; Carr D H; Chui D H
Adult hemoglobins are synthesized in erythroid colonies in vitro derived from murine circulating hemopoietic progenitor cells during embryonic development.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(9):2952-6.

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