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List of works by David H K Chui

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

scientific article

A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.

scientific article published on 28 April 2008

A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype

scientific article published on 28 May 2012

A novel monoclonal antibody based diagnostic test for alpha-thalassemia-1 carriers due to the (-SEA/) deletion

scientific article published on 01 November 1988

A novel sickle hemoglobin: hemoglobin S-south end.

scientific article

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

scientific article published on 01 December 2000

Abnormal erythroid progenitor cells in human preleukemia

scientific article published on 01 August 1982

Adult hemoglobins are synthesized in murine fetal hepatic erythropoietic cells

scientific article published on 01 December 1983

Alpha-thalassaemia and population health in Southeast Asia.

scientific article published in March 2005

Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.

scientific article published in January 2005

An electronic database of human hemoglobin variants on the World Wide Web.

scientific article published in April 1998

An ultrastructural study of early morphogenetic events during the establishment of fetal hepatic erythropoiesis

scientific article

Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity

scientific article published on 01 November 1988

BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies

scientific article published on 8 August 2008

Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion

scientific article published on 01 February 2008

Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.

scientific article

Coinheritance of alpha-thalassemia-1 and hemoglobin E/beta zero-thalassemia: practical implications for neonatal screening and genetic counseling

scientific article published on 01 May 1998

Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events

scientific article published on 17 February 2006

Diverse hematological phenotypes of β-thalassemia carriers

scientific article published on 28 April 2016

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)

scientific article published on October 2005

Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemia

scientific article published on 31 January 2019

Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion

scientific article published on 01 January 1986

Erythropoietin effects on fetal mouse erythroid cells. I. Cell population and hemoglobin synthesis ⬇️

scientific article published on December 1, 1971

Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia

scientific article published on 01 March 1993

Fetal erythropoiesis in steel mutant mice. I. A morphological study of erythroid cell development in fetal liver

scientific article published on 01 October 1974

Fetal erythropoiesis in steel mutant mice. III. Defect in differentiation from BFU-E to CFU-E during early development

scientific article published on 01 March 1978

Fetal globin gene inducers: novel agents and new potential.

scientific article published on August 2010

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin

scientific article

Fetal hemoglobin in sickle cell anemia: a glass half full?

scientific article published on 12 November 2013

Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype

scientific article

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

scientific article

Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.

scientific article published on 3 December 2011

Foetal erythropoiesis in steel mutant mice. II. Haemopoietic stem cells in foetal livers during development

scientific article published on April 1, 1975

Good practice guidelines for laboratory investigation of hemoglobinopathies.

scientific article published on January 2003

Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait

scientific article published on 01 January 2011

Hb H hydrops foetalis syndrome: a case report and review of literature.

scientific article

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

scientific article

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

scientific article published in February 2007

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

scientific article published on 01 March 2002

Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin

scientific article published on 01 July 1990

Hemoglobin H disease: not necessarily a benign disorder.

scientific article

Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.

scientific article published on January 2009

Hemoglobin SE disease in Maine, and severe thalassemia in New Hampshire.

scientific article published in April 2009

Hemoglobin SE disease: a concise review.

scientific article published on July 2007

Hemoglobin Shady Grove: a novel fetal methemoglobin variant

scientific article published on 04 March 2013

Hemoglobin ontogeny during normal mouse fetal development ⬇️

scientific article published on June 1, 1979

Hemoglobin switching during murine embryonic development: evidence for two populations of embryonic erythropoietic progenitor cells

scientific article published on 01 March 1986

Hemoglobin synthesis in siderocytes of flexed-tailed mutant (f/f) fetal mice

scientific article published on 01 July 1977

Hemoglobinopathies mimicking Hb S/β-thalassemia: Hb S/S with α-thalassemia and Hb S/Volga

scientific article published on 01 May 2006

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease

scientific article

Human ERMAP: An Erythroid Adhesion/Receptor Transmembrane Protein ⬇️

scientific article published on September 1, 2001

Human embryonic zeta-globin chain expression in deletional alpha-thalassemias

scientific article published on 01 July 1992

Human embryonic zeta-globin gene expression in mouse-human hybrid erythroid cell lines

scientific article published on 01 August 1995

Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

scientific article published on April 1998

Identification of an extensive zeta-alpha globin gene deletion in a Chinese individual

scientific article published on 01 March 1992

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

scientific article

Induced pluripotent stem cell-based mapping of β-globin expression throughout human erythropoietic development

scientific article published on 01 August 2018

Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency?

scientific article published on 31 October 2011

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.

scholarly article

Massive splenic infarction in an adolescent with hemoglobin S-HPFH

scientific article published on 31 December 2012

Murine Hn1 on chromosome 11 is expressed in hemopoietic and brain tissues.

scientific article published in September 1997

New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].

scientific article published in January 2010

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

scientific article published on 15 June 2013

PhenCode: connecting ENCODE data with mutations and phenotype

scientific article

Prenatal diagnosis of hemoglobinopathies in Ontario, Canada

scientific article published on 01 January 2005

Prenatal exclusion of β thalassaemia major by examination of maternal plasma

scientific article published in The Lancet

Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screening

scientific article published on 01 May 1997

Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation ⬇️

scientific article published on May 1, 1980

Pulse oximetry screening for critical congenital heart defects

scientific article published on 01 October 2012

Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster

article

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?

scientific article

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

scientific article

Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.

scientific article published in February 2005

Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 alpha-globin gene triplications.

scientific article

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

scientific article

The clinical severity of hemoglobin S/Black ((A) γδβ)(0) -thalassemia

scientific article published on 28 April 2017

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes

scientific article published on 13 January 2016

Unequal alpha and beta globin mRNA in reticulocytes of normal and mutant f/f fetal mice

scientific article published on 01 March 1980

Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: a systematic review.

scientific article

Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong.

scientific article published in June 2008

cDNA cloning of murine Nrf 2 gene, coding for a p45 NF-E2 related transcription factor.

scientific article published on April 1995

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