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Title	Author(s)	Issue Date
Haemoglobin H disease due to (--SEA) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: A family study Journal:Clinical and Laboratory Haematology, Supplement	Ma, SK Chan, AYY Chiu, EKW Chan, LC	2001
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
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
Hb Kodaira II: a high oxygen affinity variant with a novel mutation in the β-globin gene and phenotypic identity to Hb Kodaira Journal:Hemoglobin	So, CC Ma, SK Law, KM Chan, AYY Chan, LC Wong, KF	2002
Interaction between (-SEA) α-thalassemla deletion and uncommon non-deletional α-globin gene mutations in Chinese patients Journal:Haematologica	Ma, ESK De Chow, EY Chan, AYY Chan, LC	2001
Inversion (14)(q11q32) in childhood T-cell acute lymphoblastic leukemia Journal:Cancer Genetics and Cytogenetics	Kwong, YL Shing, MK Wan, TM Yuen, PMP Chan, AYY Wong, KF Chan, LC	1994
A laboratory strategy for genotyping haemoglobin H disease in the Chinese Journal:Journal of Clinical Pathology	Chan, AYY So, CC Ma, ESK Chan, LC	2007
The lack of association between JAK2 V617F mutation and myelodysplastic syndrome with or without myelofibrosis [4] Journal:Leukemia	Yip, SF So, CC Chan, AyY Liu, HsY Wan, TsK Chan, LC	2006
Low affinity and unstable hemoglobin variant caused by AAC→ATC (Asn→Ile) mutation at codon 108 of the β-globin gene [3] Journal:Haematologica	Ma, ESK Chow, EYD Chan, AYY Chu, CM Lin, SY Chan, LC	2002
Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype Journal:Clinical Neurology and Neurosurgery	Au, LWC Lee, HCH Sheng, B Chan, KY Yau, EKC Mak, MC Chan, AYW Chan, AYY Lau, CKY Mok, VCT Lam, CW	2020
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
Myelodysplastic syndrome with myelofibrosis and basophilia : Detection of trisomy 8 in basophils by fluorescence in-situ hybridization Journal:Leukemia and Lymphoma	Ma, SK Chan, JCW Wan, TSK Chan, AYY Chan, LC	1998
Near-octaploidy in essential thrombocythemia Journal:Cancer Genetics and Cytogenetics	Kwong, YL Chan, AYY Wei, D Chan, LC	1993
Near-triploid myeloblastic transformation of chronic myeloid leukemia with bizarre blast morphology Journal:Cancer Genetics and Cytogenetics	Kwong, YL Chan, AYY Chan, LC Wong, KF Chu, YC	1992
A novel AATAAA→CATAAA mutation at the polyadenylation site of the β-globin gene [3] Journal:British Journal of Haematology	Ma, SK Lee, ACW Chan, AYY Chan, LC	2001
A novel beta-delta globin gene fusion leads to over-expression of delta globin chain and a mild thalassemia intermedia phenotype when co-inherited with beta-zero thalassemia Proceeding/Conference:Blood	So, JCC Chan, AYY Tsang, STY Lee, ACW Au, WY Ma, ESK Chan, LC	2006
A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with β0-thalassaemia Journal:British Journal of Haematology	So, CC Chan, AYY Tsang, STY Lee, ACW Au, WY Ma, ESK Chan, LC	2007
Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease Journal:Hemoglobin	So, JCC Chan, AYY Ma, ESK	2014
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
Screening for (-(SEA)) α-globin gene deletion in β-thalassemia carriers and prevention of hydrops fetalis Journal:Haematologica	Ma, ESK Chan, AYY Shau Yin Ha Chan, GCF Yu Lung Lau Li Chong Chan	2000

Showing results 13 to 32 of 43 < previous next >