Siu V - Search Results

1

An interstitial deletion of the long arm of chromosome 21 in a case of a first episode of psychosis.

Takhar J, Malla AK, Siu V, MacPherson C, Fan YS, Townsend L. Takhar J, et al. Among authors: siu v. Acta Psychiatr Scand. 2002 Jul;106(1):71-4; discussion 74-5. doi: 10.1034/j.1600-0447.2002.01323.x. Acta Psychiatr Scand. 2002. PMID: 12100350

2

Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements.

Fan YS, Siu VM, Jung JH, Xu J. Fan YS, et al. Among authors: siu vm. Genet Test. 2000;4(1):9-14. doi: 10.1089/109065700316417. Genet Test. 2000. PMID: 10794355

3

Brief report: A case of autism with interstitial deletion of chromosome 13.

Steele MM, Al-Adeimi M, Siu VM, Fan YS. Steele MM, et al. Among authors: siu vm. J Autism Dev Disord. 2001 Apr;31(2):231-4. doi: 10.1023/a:1010759401344. J Autism Dev Disord. 2001. PMID: 11450821

4

Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.

Fan YS, Siu VM. Fan YS, et al. Among authors: siu vm. Am J Med Genet. 2001 Aug 15;102(3):266-71. doi: 10.1002/ajmg.1460. Am J Med Genet. 2001. PMID: 11484205

5

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.

Fan YS, Zhang Y, Speevak M, Farrell S, Jung JH, Siu VM. Fan YS, et al. Among authors: siu vm. Genet Med. 2001 Nov-Dec;3(6):416-21. doi: 10.1097/00125817-200111000-00007. Genet Med. 2001. PMID: 11715006 Free article.

6

Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.

Fan YS, Siu VM, Jung JH, Farrell SA, Côté GB. Fan YS, et al. Among authors: siu vm. Am J Med Genet. 2001 Oct 15;103(3):231-4. doi: 10.1002/ajmg.1534.abs. Am J Med Genet. 2001. PMID: 11745996

7

Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions.

Uddin RK, Zhang Y, Siu VM, Fan YS, O'Reilly RL, Rao J, Singh SM. Uddin RK, et al. BMC Med Genet. 2006 Mar 2;7:18. doi: 10.1186/1471-2350-7-18. BMC Med Genet. 2006. PMID: 16512914 Free PMC article.

8

A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: is this a candidate region for the syndrome?

Xu J, Fan YS, Siu VM. Xu J, et al. Among authors: siu vm. Am J Med Genet A. 2008 Jul 15;146A(14):1886-9. doi: 10.1002/ajmg.a.32359. Am J Med Genet A. 2008. PMID: 18553512 No abstract available.

9

Choroideremia associated with an X-autosomal translocation.

Siu VM, Gonder JR, Jung JH, Sergovich FR, Flintoff WF. Siu VM, et al. Hum Genet. 1990 Apr;84(5):459-64. doi: 10.1007/BF00195820. Hum Genet. 1990. PMID: 2323779 Free PMC article.

10

Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia.

Farhan SM, Murphy LM, Robinson JF, Wang J, Siu VM, Rupar CA, Prasad AN; FORGE Canada Consortium; Hegele RA. Farhan SM, et al. Epilepsia. 2014 Sep;55(9):e106-11. doi: 10.1111/epi.12730. Epub 2014 Jul 24. Epilepsia. 2014. PMID: 25060828 Free article.

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