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	Title	Author(s)	Issue Date	Views
	Comparison of haemoglobin H inclusion bodies with embryonic ζ globin in screening for α thalassaemia Journal:Journal of Clinical Pathology	Chan, LC So, JCC Chui, DHK	1995	118
	Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5] Journal:British Journal of Haematology	Ma, SK Chan, AYY Chan, LC Chui, DHK Waye, JS	2000	48
	Diagnostic pitfall in PCR-based α-thalassemia genotyping resulting from a (G→C) polymorphism at nucleotide 71 3′ to the α2-globin gene termination codon [2] Journal:Clinical Chemistry	Chan, AYY Luo, HY Wang, W Chui, DHK Ma, ESK Chan, LC Chong, SS	2006
	Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures Journal:Prenatal Diagnosis	Lau, ET Kwok, YK Chui, DHK Wong, HS Luo, HY Tang, MHY	2001	71
	Genotype-phenotype correlation of b-thalassemia patients in Hong Kong Proceeding/Conference:International Conference on Thalassaemia and the Haemoglobinopathies	Ma, ESK Ha, SY Chan, AYY Chan, GCF Chan, LC Chui, DHK	1999	139
	Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family Journal:Clinical and Laboratory Haematology	Leung, KFS Au, WY Chan, AYY Chan, LC Waye, JS Chui, DHK Ma, SK	2001	189
	Hb A2 Hong Kong - A novel δ-globin variant in a chinese family masks the diagnosis of β-thalassemia trait Journal:Hemoglobin	So, CC Chan, AYY Luo, HY Verhovsek, M Chui, DHK Ling, SC Chan, LC	2011	178
	Hemoglobin H disease: Not necessarily a benign disorder Journal:Blood	Chui, DHK Fucharoen, S Chan, V	2003	190
	Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency? Journal:American Journal of Hematology	Verhovsek, M So, JCC O'Shea, T Gibney, GT Ma, ESK Steinberg, MH Chui, DHK	2012	143
	MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis Journal:Proceedings of the National Academy of Sciences of the United States of America	Ding, C Chiu, RWK Lau, TK Leung, TN Chan, LC Chan, AYY Charoenkwan, P Ng, ISL Law, HY Ma, ESK Xu, X Wanapirak, C Sanguansermsri, T Liao, C Tan Jin Ai, MA Chui, DHK Cantor, CR Lo, YMD	2004
	Prenatal detection of Hb Barts Disease in Maternal Blood Proceeding/Conference:International Conference on Prenatal Diagnosis & Therapy, ISPD 2004	Lau, ET Kwok, YK Chui, DHK Luo, HY Leung, KY Lee, CP Lam, YH Tang, MHY	2004
	Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening Journal:New England Journal of Medicine	Lau, YL Chan, LC Chan, YYA Ha, SY Yeung, CY Waye, JS Chui, DHK	1997	257
	Routine screening of (--SEA) α-thalassemia deletion by an enzyme-linked immunosorbent assay for embryonic ζ-globin chains Journal:Acta Haematologica	Ma, SK Ma, V Chan, AYY Chan, LC Chui, DHK	2002	206
	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:Journal of Clinical Pathology	Chan, LC Ma, SK Chan, AYY Ha, SY Waye, JS Lau, YL Chui, DHK	2001	213
	Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Journal:American Journal of Hematology	Koenig, SC Becirevic, E Hellberg, MSC Li, MY So, JCC Hankins, JS Ware, RE Mcmahon, L Steinberg, MH Luo, HY Chui, DHK	2009
	Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood Journal:Prenatal Diagnosis	Lau, ET Kwok, YK Luo, HY Leung, KY Lee, CP Lam, YH Chui, DHK Tang, MHY	2005	77
	Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications Journal:Clinical Chemistry	Wang, W Ma, ESK Chan, AYY Prior, J Erber, WN Chan, LC Chui, DHK Chong, SS	2003	211
	Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong Journal:American Journal of Hematology	Gibney, GT Panhuysen, CIM So, JCC Ma, ESK Shau, YH Chi, KL Lee, ACW Chi, KL Hui, LY Yu, LL Johnson, DM Farrell, JJ Bisbee, AB Farrer, LA Steinberg, MH Li, CC Chui, DHK	2008
	β-Thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (-CTTT) β0-thalassemia mutation Journal:American Journal of Hematology	Ma, SK Chow, EYD Chan, AYY Kung, NNS Waye, JS Chan, LC Chui, DHK	2000	200

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