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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionFarrell, 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, DHK2011183
Hb A2 Hong Kong - A novel δ-globin variant in a chinese family masks the diagnosis of β-thalassemia traitSo, CC; Chan, AYY; Luo, HY; Verhovsek, M; Chui, DHK; Ling, SC; Chan, LC2011193
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patientsKoenig, SC; Becirevic, E; Hellberg, MSC; Li, MY; So, JCC; Hankins, JS; Ware, RE; Mcmahon, L; Steinberg, MH; Luo, HY; Chui, DHK2009117
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, SS200662
Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal bloodLau, ET; Kwok, YK; Luo, HY; Leung, KY; Lee, CP; Lam, YH; Chui, DHK; Tang, MHY200570
Prenatal detection of Hb Barts Disease in Maternal BloodLau, ET; Kwok, YK; Chui, DHK; Luo, HY; Leung, KY; Lee, CP; Lam, YH; Tang, MHY200439
Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell culturesLau, ET; Kwok, YK; Chui, DHK; Wong, HS; Luo, HY; Tang, MHY200167
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