Kee SK - Search Results

1

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

Lim AS, Lim TH, Kee SK, Chia P, Raman S, Eu EL, Lim JY, Tien SL. Lim AS, et al. Among authors: kee sk. Ann Acad Med Singap. 2008 Jul;37(7):594-7. Ann Acad Med Singap. 2008. PMID: 18695774 Free article. Review.

2

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.

Lim AS, Lim TH, Kee SK, Chieng R, Tay SK. Lim AS, et al. Among authors: kee sk. Am J Med Genet A. 2003 Mar 1;117A(2):172-6. doi: 10.1002/ajmg.a.10893. Am J Med Genet A. 2003. PMID: 12567417

3

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

Lim AS, Chia P, Kee SK, Raman S, Tien SL. Lim AS, et al. Among authors: kee sk. Ann Acad Med Singap. 2004 Jul;33(4):537-40. Ann Acad Med Singap. 2004. PMID: 15329773 Free article.

4

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

Lim AS, Lim TH, Hess MM, Kee SK, Lau YY, Gilbert R, Hempel TE, Anderson KJ, Zaleski DH, Tien SL, Chia P, Subramaniam R, Tan HK, Tan AS, Sanger WG. Lim AS, et al. Among authors: kee sk. Hong Kong Med J. 2010 Dec;16(6):427-33. Hong Kong Med J. 2010. PMID: 21135418 Free article.

5

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

Kee SK, See VH, Chia P, Tan WC, Tien SL, Lim ST. Kee SK, et al. J Pediatr Genet. 2013 Mar;2(1):37-41. doi: 10.3233/PGE-13046. J Pediatr Genet. 2013. PMID: 27625838 Free PMC article.

6

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

Lau LC, Kee SK, Tien SL, Koh Mickey BC. Lau LC, et al. Among authors: kee sk. Cancer Genet Cytogenet. 2007 Jan 1;172(1):66-9. doi: 10.1016/j.cancergencyto.2006.05.019. Cancer Genet Cytogenet. 2007. PMID: 17175382

7

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

Gibbons B, Tan SY, Kee SK, Quaife R, Lim ST. Gibbons B, et al. Among authors: kee sk. Am J Med Genet. 1999 Sep 17;86(3):289-93. Am J Med Genet. 1999. PMID: 10482883 Review.

8

Integration-free induced pluripotent stem cells from three endangered Southeast Asian non-human primate species.

Bao Q, Tay NL, Lim CY, Chua DHH, Kee SK, Choolani M, Loh YH, Ng SC, Chai C. Bao Q, et al. Among authors: kee sk. Sci Rep. 2024 Jan 29;14(1):2391. doi: 10.1038/s41598-023-50510-9. Sci Rep. 2024. PMID: 38287040 Free PMC article.

9

Unusual gallbladder disease: spontaneous gallbladder haematoma.

Kee SK, Je D, Nho WY. Kee SK, et al. Hong Kong Med J. 2022 Jun;28(3):270.e1-270.e3. doi: 10.12809/hkmj219569. Hong Kong Med J. 2022. PMID: 35765736 Free article. No abstract available.

10

A comparative analysis of gallbladder torsion and acute gallbladder disease without torsion: a single-center retrospective case series study.

Nho WY, Kim JK, Kee SK. Nho WY, et al. Among authors: kee sk. Ann Transl Med. 2021 Sep;9(18):1399. doi: 10.21037/atm-21-2399. Ann Transl Med. 2021. PMID: 34733951 Free PMC article.

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