P. Chia

The importance of high resolution chromosome analysis in the diagnosis of birth defects: case reports of holoproscencephaly and cystic hygroma.

S. Tien, A. Lim, S. Kee, 2004, Annals of the Academy of Medicine, Singapore.

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 aneuploidy screening with fluorescence in-situ hybridisation: is it a sufficiently robust stand-alone test for prenatal diagnosis?

W. Sanger, S. Tien, T. Lim, 2010, Hong Kong medical journal = Xianggang yi xue za zhi.

A case of pure partial duplication 3q in a fetus due to a maternally inherited der(5)ins(5;3)(q33.1;q26.2q27) delineated by FISH

S. Tien, D. Pickering, T. Lim, 2004, Prenatal diagnosis.

Holoprosencephaly: an antenatally-diagnosed case series and subject review.

S. Tien, T. Lim, A. Lim, 2008, Annals of the Academy of Medicine, Singapore.

Differential outcomes in an extended family with constitutional t(11;22)(q23.3;q11.2)

S. Tien, W. Tan, S. Kee, 2013, Journal of Pediatric Genetics.