Y. Wee

发表

Molecular characterisation of Haemoglobin Constant Spring and Haemoglobin Quong Sze with a Combine-Amplification Refractory Mutation System.

Jin Ai Mary Anne Tan, K. Chua, E. George, 2009, The Malaysian journal of medical sciences : MJMS.

Interaction of Hb South Florida (codon 1; GTG→ATG) and HbE, with β-thalassemia (IVS1-1; G→A): expression of different clinical phenotypes

Jin Ai Mary Anne Tan, L. Chan, E. George, 2009, European Journal of Pediatrics.

Combine-ARMS: a rapid and cost-effective protocol for molecular characterization of beta-thalassemia in Malaysia.

M. Thong, S. Yap, J. Tan, 2001, Genetic testing.

High Prevalence of Alpha- and Beta-Thalassemia in the Kadazandusuns in East Malaysia: Challenges in Providing Effective Health Care for an Indigenous Group

Jin Ai Mary Anne Tan, K. Chua, Ping-Chin Lee, 2010, Journal of biomedicine & biotechnology.

Alpha-Thalassaemia in Association with Beta-Thalassaemia Patients in Malaysia: A Study on the Co-Inheritance of Both Disorders

S. Yap, E. George, P. Tan, 2008, Public Health Genomics.

Heterogeneity in α‐thalassemia interactions in Malays, Chinese and Indians in Malaysia

Jin Ai Mary Anne Tan, S. Yap, T. Chow, 2005 .

Rapid and cost-effective antenatal diagnosis of haemoglobin Bart's hydrops foetalis syndrome using a duplex-polymerase chain reaction.

S. Yap, J. Tan, P. Tan, 2005, The Medical journal of Malaysia.

Identification of α°-thalassaemia (–SEA) using an enzyme-linked immunosorbent assay (ELISA) for embryonic zeta-globin chain detection – a preliminary study

Z. Zakaria, R. Hassan, E. George, 2006 .

Heterogeneity in alpha-thalassemia interactions in Malays, Chinese and Indians in Malaysia.

Jin Ai Mary Anne Tan, S. Yap, T. Chow, 2005, The journal of obstetrics and gynaecology research.

Mild Beta-Thalassemia intermedia Caused by Compound Heterozygosity for Gγ(Aγδβ)o/β-Thalassemia and Molecular Characterization of the Defect in Four Chinese Families

S. Yap, Y. Wee, K. Tan, 2003, Acta Haematologica.

Mild beta-thalassemia intermedia caused by compound heterozygosity for (G)gamma((A)gammadeltabeta)(o)/beta-thalassemia and molecular characterization of the defect in four Chinese families.

S. Yap, Y. Wee, K. Tan, 2003, Acta haematologica.

190 Complete Genome Sequences and Papillomavirus 6 Based on 724 Isolates Global Genomic Diversity of Human

K. Seme, A. Fiander, E. Franco, 2014 .

Thalassemia intermedia in HbH-CS disease with compound heterozygosity for beta-thalassemia: challenges in hemoglobin analysis and clinical diagnosis.

Jin Ai Mary Anne Tan, E. George, Y. Wee, 2009, Genes & genetic systems.