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Browsing by Author Chan, AYY
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Showing results 28 to 43 of 43
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Title
Author(s)
Issue Date
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Clinical phenotype of haemoglobin Q-H disease
Journal:
Journal of Clinical Pathology
Leung, KFS
Ma, ESK
Chan, AYY
Chan, LC
2004