Yong MH - Search Results

1

De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability.

Brett MS, Ng IS, Lim EC, Yong MH, Li Z, Lai A, Tan EC. Brett MS, et al. Among authors: yong mh. Gene. 2013 Mar 15;517(1):82-8. doi: 10.1016/j.gene.2012.12.082. Epub 2013 Jan 11. Gene. 2013. PMID: 23313878

2

Del(3) (p25.3) without phenotypic effect.

Knight LA, Yong MH, Tan M, Ng IS. Knight LA, et al. Among authors: yong mh. J Med Genet. 1995 Dec;32(12):994-5. doi: 10.1136/jmg.32.12.994. J Med Genet. 1995. PMID: 8825934 Free PMC article.

3

Subtle translocation (18;21) confirmed by FISH in a patient with Down syndrome.

Knight LA, Yong MH, Tan M, Ng IS. Knight LA, et al. Among authors: yong mh. Clin Genet. 1996 Nov;50(5):430-2. doi: 10.1111/j.1399-0004.1996.tb02402.x. Clin Genet. 1996. PMID: 9007338

4

Williams syndrome--the Singapore General Hospital experience.

Teo SH, Chan DK, Yong MH, Ng IS, Wong KY, Knight L, Ho LY. Teo SH, et al. Among authors: yong mh. Ann Acad Med Singap. 1997 May;26(3):360-4. Ann Acad Med Singap. 1997. PMID: 9285033

5

De novo trisomy 12p in twin girls with different levels of mosaicism.

Lim EC, Ng IS, Yong MH, Yon HY, Brett MS, Tan EC. Lim EC, et al. Among authors: yong mh. Am J Med Genet A. 2013 Jul;161A(7):1702-5. doi: 10.1002/ajmg.a.35943. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686734

6

Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.

Tan ES, Yong MH, Lim EC, Li ZH, Brett MS, Tan EC. Tan ES, et al. Among authors: yong mh. Mol Cytogenet. 2014 May 16;7:32. doi: 10.1186/1755-8166-7-32. eCollection 2014. Mol Cytogenet. 2014. PMID: 24959201 Free PMC article.

7

Partial monosomy for chromosome 22 in a girl with mental retardation.

Yong YP, Knight LA, Yong MH, Lam S, Ho LY. Yong YP, et al. Among authors: yong mh. Singapore Med J. 1997 Feb;38(2):85-6. Singapore Med J. 1997. PMID: 9269370

8

Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.

Choo S, Teo SH, Tan M, Yong MH, Ho LY. Choo S, et al. Among authors: yong mh. J Perinatol. 2002 Jul-Aug;22(5):420-3. doi: 10.1038/sj.jp.7210712. J Perinatol. 2002. PMID: 12082482

9

Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore.

Yong MH, Hwang WS, Knight LA, Fung W, Chan MY, Seow WT, Chui CH. Yong MH, et al. Singapore Med J. 2009 Nov;50(11):1090-4. Singapore Med J. 2009. PMID: 19960166 Free article.

10

Highly complex chromosomal rearrangement of chromosome 9 in a case of chronic myeloid leukemia.

Lau LC, Knight L, Tien SL, Lim P, Yong MH, Chong YY. Lau LC, et al. Among authors: yong mh. Cancer Genet Cytogenet. 1998 Jul 15;104(2):153-6. doi: 10.1016/s0165-4608(97)00451-2. Cancer Genet Cytogenet. 1998. PMID: 9666810

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