| Title | Author(s) | Year | View Count |
 | Detection of a small novel deletion in the α-globin gene and type II -α 3.7 deletion by heteroduplex formation | Chan, AYY; ShiuKwan, E; Au, WY; Chow, EYD; Chan, LC | 2002 | 56 |
 | Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? | Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK | 2001 | 330 |
| A novel AATAAA→CATAAA mutation at the polyadenylation site of the β-globin gene [3] | Ma, SK; Lee, ACW; Chan, AYY; Chan, LC | 2001 | 58 |
| Haemoglobin H disease due to (--SEA) α-globin gene deletion and α2-codon 30 (ΔGAG) mutation: A family study | Ma, SK; Chan, AYY; Chiu, EKW; Chan, LC | 2001 | 68 |
| Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family | Leung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK | 2001 | 65 |
| Interaction between (-SEA) α-thalassemla deletion and uncommon non-deletional α-globin gene mutations in Chinese patients | Ma, ESK; De Chow, EY; Chan, AYY; Chan, LC | 2001 | 60 |
| Thalassemia screening based on red cell indices in the Chinese | Ma, ESK; Chan, AYY; Yin Ha, S; Lau, YL; Chan, LC | 2001 | 93 |
| Two novel β-thalassemia alleles in the chinese: The IVS-II-2 (-T) and nucleotide +8 (C→T) β-globin gene mutations | Ma, SK; Ha, SY; Chan, AYY; Chan, GCF; Lau, YL; Chan, LC | 2000 | 48 |
| Compound heterozygosity for triplicated α-globin gene and (- -(SEA)) α-globin gene deletion: Implication for thalassaemia screening [5] | Ma, SK; Chan, AYY; Chan, LC; Chui, DHK; Waye, JS | 2000 | 55 |
| β-Thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (-CTTT) β0-thalassemia mutation | Ma, SK; Chow, EYD; Chan, AYY; Kung, NNS; Waye, JS; Chan, LC; Chui, DHK | 2000 | 115 |
 | Screening of a-thalassemia in b-thalassemia Carriers and Prevention of Hydrops Fetails | Ma, ESK; Chan, AYY; Ha, SY; Chan, GCF; Lau, YL; Chan, LC | 2000 | 67 |
| Thalassaemia Screening in Hong Kong Strategies and Potential Pitfalls | Ma, ESK; Chan, AYY; Ha, SY; Chan, GCF; Lau, YL; Chan, LC | 2000 | 60 |
| Screening for (-(SEA)) α-globin gene deletion in β-thalassemia carriers and prevention of hydrops fetalis | Ma, ESK; Chan, AYY; Shau Yin Ha; Chan, GCF; Yu Lung Lau; Li Chong Chan | 2000 | 56 |
| Genotype-phenotype correlation of b-thalassemia patients in Hong Kong | Ma, ESK; Ha, SY; Chan, AYY; Chan, GCF; Chan, LC; Chui, DHK | 1999 | 85 |
| Two Novel b-thalassemia alleles in the Chinese: IVSII-2(-T) b-Zero Mutation and NT+8 (C - T) Silent b-Plus Mutation | Ma, ESK; Chan, AYY; Ha, SY; Chan, GCF; Chan, LC | 1999 | 65 |
| Myelodysplastic syndrome with myelofibrosis and basophilia : Detection of trisomy 8 in basophils by fluorescence in-situ hybridization | Ma, SK; Chan, JCW; Wan, TSK; Chan, AYY; Chan, LC | 1998 | 84 |
| Comparison of the HbH inclusion test and a PCR test in routine screening for α thalassaemia in Hong Kong | Chan, AYY; So, CKC; Chan, LC | 1996 | 279 |
| Inversion (14)(q11q32) in childhood T-cell acute lymphoblastic leukemia | Kwong, YL; Shing, MK; Wan, TM; Yuen, PMP; Chan, AYY; Wong, KF; Chan, LC | 1994 | 63 |
| Cytogenetic triclonality in acute myeloid leukemia: A morphologic, immunologic and in situ hybridization study | Kwong, YL; Lam, CK; Chan, AYY; Lie, AKW; Chan, LC | 1994 | 76 |
| Near-octaploidy in essential thrombocythemia | Kwong, YL; Chan, AYY; Wei, D; Chan, LC | 1993 | 58 |
|
