| Title | Author(s) | Year | View Count |  | Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency? | Verhovsek, M; So, JCC; O'Shea, T; Gibney, GT; Ma, ESK; Steinberg, MH; Chui, DHK | 2012 | 85 |
| A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression | Farrell, JJ; Sherva, RM; Chen, ZY; Luo, HY; Chu, BF; Ha, SY; Li, CK; Lee, ACW; Li, RCH; Li, CK; Yuen, HL; So, JCC; Ma, ESK; Chan, LC; Chan, V; Sebastiani, P; Farrer, LA; Baldwin, CT; Steinberg, MH; Chui, DHK | 2011 | 167 |
| Hb A2 Hong Kong - A novel δ-globin variant in a chinese family masks the diagnosis of β-thalassemia trait | So, CC; Chan, AYY; Luo, HY; Verhovsek, M; Chui, DHK; Ling, SC; Chan, LC | 2011 | 163 |
| Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients | Koenig, SC; Becirevic, E; Hellberg, MSC; Li, MY; So, JCC; Hankins, JS; Ware, RE; Mcmahon, L; Steinberg, MH; Luo, HY; Chui, DHK | 2009 | 87 |
| BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies | Sedgewick, AE; Timofeev, N; Sebastiani, P; So, JCC; Ma, ESK; Chan, LC; Fucharoen, G; Fucharoen, S; Barbosa, CG; Vardarajan, BN; Farrer, LA; Baldwin, CT; Steinberg, MH; Chui, DHK | 2008 | 95 |
| Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong | 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 | 129 |
| 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] | Chan, AYY; Luo, HY; Wang, W; Chui, DHK; Ma, ESK; Chan, LC; Chong, SS | 2006 | 60 |
| Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood | Lau, ET; Kwok, YK; Luo, HY; Leung, KY; Lee, CP; Lam, YH; Chui, DHK; Tang, MHY | 2005 | 40 |
 | Prenatal detection of Hb Barts Disease in Maternal Blood | Lau, ET; Kwok, YK; Chui, DHK; Luo, HY; Leung, KY; Lee, CP; Lam, YH; Tang, MHY | 2004 | 29 |
 | MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis | 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 | 236 |
| Hemoglobin H disease: Not necessarily a benign disorder | Chui, DHK; Fucharoen, S; Chan, V | 2003 | 123 |
| Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 α-globin gene triplications | Wang, W; Ma, ESK; Chan, AYY; Prior, J; Erber, WN; Chan, LC; Chui, DHK; Chong, SS | 2003 | 64 |
| Routine screening of (--SEA) α-thalassemia deletion by an enzyme-linked immunosorbent assay for embryonic ζ-globin chains | Ma, SK; Ma, V; Chan, AYY; Chan, LC; Chui, DHK | 2002 | 93 |
| 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? | Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK | 2001 | 338 |
| Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures | Lau, ET; Kwok, YK; Chui, DHK; Wong, HS; Luo, HY; Tang, MHY | 2001 | 44 |
| Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family | Leung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK | 2001 | 73 |
| 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 | Ma, SK; Chow, EYD; Chan, AYY; Kung, NNS; Waye, JS; Chan, LC; Chui, DHK | 2000 | 131 |
| Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5] | Ma, SK; Chan, AYY; Chan, LC; Chui, DHK; Waye, JS | 2000 | 60 |
| Genotype-phenotype correlation of b-thalassemia patients in Hong Kong | Ma, ESK; Ha, SY; Chan, AYY; Chan, GCF; Chan, LC; Chui, DHK | 1999 | 90 |
| Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong - Implications for population screening | Lau, YL; Chan, LC; Chan, YYA; Ha, SY; Yeung, CY; Waye, JS; Chui, DHK | 1997 | 672 |
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