| Title | Author(s) | Year | View Count |
 | 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 | 159 |
| 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 | 152 |
| 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 | 79 |
| 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 | 56 |
| 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 | 30 |
 | 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 | 23 |
| 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 | 36 |
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