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Showing results 13 to 21 of 21 < previous

	Title	Author(s)	Issue Date
	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
	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
	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
	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
	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
	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

Showing results 13 to 21 of 21 < previous