P. Tan

Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms

K. Chua, J. Tan, E. George, 2015, BMJ Open.

Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms

K. Chua, J. Tan, E. George, 2015, BMJ Open.

A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population

Kok Siong Poon, K. Tan, P. Tan, 2022, BMC research notes.

Molecular defects in the β-globin gene identified in different ethnic groups/populations during prenatal diagnosis for β-thalassemia: a Malaysian experience

S. Yap, R. Chandran, J. Tan, 2004, Clinical and Experimental Medicine.

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.

Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience.

S. Yap, R. Chandran, J. Tan, 2004, Clinical and experimental medicine.

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.