S. Kee

Sperm segregation patterns by fluorescence in situ hybridization studies of a 46,XY,t(2;6) heterozygote giving rise to a rare triploid product of conception with a 69,XXY,t(2;6)(p12;q24)der(6)t(2;6)(p12;q24)pat karyotype

T. Lim, A. Lim, S. Tay, 2002, American journal of medical genetics. Part A.

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.

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.

Short communication Trisomy 8 as sole cytogenetic abnormality in a case of chronic lymphocytic leukemia

S. Tien, L. Lau, B. Mickey, 2007 .

Trisomy 8 as sole cytogenetic abnormality in a case of chronic lymphocytic leukemia.

S. Tien, L. Lau, S. Kee, 2007, Cancer genetics and cytogenetics.

Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).

S. Tan, B. Gibbons, S. T. Lim, 1999, American journal of medical genetics.

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.