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Title	Author(s)	Issue Date	Views
Clinical phenotype of haemoglobin Q-H disease Journal:Journal of Clinical Pathology	Leung, KFS Ma, ESK Chan, AYY Chan, LC	2004
Comparison of the HbH inclusion test and a PCR test in routine screening for α thalassaemia in Hong Kong Journal:Journal of Clinical Pathology	Chan, AYY So, CKC Chan, LC	1996	97
Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5] Journal:British Journal of Haematology	Ma, SK Chan, AYY Chan, LC Chui, DHK Waye, JS	2000	48
Cytogenetic triclonality in acute myeloid leukemia: A morphologic, immunologic and in situ hybridization study Journal:Cancer Genetics and Cytogenetics	Kwong, YL Lam, CK Chan, AYY Lie, AKW Chan, LC	1994	139
Deletion 12p in de novo acute myeloid leukemia: An association with early progenitor cell Journal:Cancer Genetics and Cytogenetics	Chan, LC Kwong, YL Liu, HW Lee, CP Lie, KW Chan, AYY	1992	127
Detection and characterisation of β-globin gene cluster deletions in Chinese using multiplex ligationdependent probe amplification Journal:Journal of Clinical Pathology	So, CC So, ACY Chan, AYY Tsang, STY Ma, ESK Chan, LC	2009
Detection of a small novel deletion in the α-globin gene and type II -α 3.7 deletion by heteroduplex formation Journal:Hemoglobin	Chan, AYY ShiuKwan, E Au, WY Chow, EYD Chan, LC	2002	54
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] Journal:Clinical Chemistry	Chan, AYY Luo, HY Wang, W Chui, DHK Ma, ESK Chan, LC Chong, SS	2006
Double heterozygosity for Hb New York [β113 GTG→GAG; VAL→GLU] and β°-thalassemia mutations manifests as a thalassemia trait Journal:Pediatric Hematology and Oncology	Lee, ACW Ma, ESK Chan, AYY Szeto, SC Chan, LC	2008	84
The Effect of Mild b-thalassaemia Mutations on Clinical Mainfestation of b-thalassaemia Major and Intermedia in Chinese Proceeding/Conference:Guangdong-Hong Kong 2004 Paediatrics Exchange Meeting	Chen, JF Ma, ESK Ha, SY Chan, GCF Chan, AYY Chan, LC Lau, YL	2004
The Effect of Mild b-Thalassaemia Mutations on Clinical Manifestation of b-Thalassaemia Major and Intermedia in Chinese Proceeding/Conference:Hong Kong Journal of Paediatrics	Chen, JF Ma, ESK Ha, SY Chan, GCF Chan, AYY Chan, LC Lau, YL	2004	94
Genotype-phenotype correlation of b-thalassemia patients in Hong Kong Proceeding/Conference:International Conference on Thalassaemia and the Haemoglobinopathies	Ma, ESK Ha, SY Chan, AYY Chan, GCF Chan, LC Chui, DHK	1999	139
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	152
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	189
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	178
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	170
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	148
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	127
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	185

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