Cheung SW - Search Results

1

Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.

Breman AM, Probst FJ, Blazo MA, Schaaf CP, Roney EK, Craigen WJ, Bacino CA, Cheung SW. Breman AM, et al. Among authors: cheung sw. Am J Med Genet A. 2011 Jun;155A(6):1465-8. doi: 10.1002/ajmg.a.33935. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567909 Free PMC article. No abstract available.

2

Introductory comments on special section-genomic microduplications: When adding may equal subtracting.

Bacino CA, Cheung SW. Bacino CA, et al. Among authors: cheung sw. Am J Med Genet A. 2010 May;152A(5):1063-5. doi: 10.1002/ajmg.a.33346. Am J Med Genet A. 2010. PMID: 20425812

3

A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome.

Holder JL Jr, Lotze TE, Bacino C, Cheung SW. Holder JL Jr, et al. Among authors: cheung sw. Am J Med Genet A. 2012 Aug;158A(8):1962-6. doi: 10.1002/ajmg.a.35289. Epub 2012 Apr 9. Am J Med Genet A. 2012. PMID: 22488736

4

4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.

Bi W, Cheung SW, Breman AM, Bacino CA. Bi W, et al. Among authors: cheung sw. Am J Med Genet A. 2016 Oct;170(10):2540-50. doi: 10.1002/ajmg.a.37796. Epub 2016 Jun 10. Am J Med Genet A. 2016. PMID: 27287194

5

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

Wat MJ, Shchelochkov OA, Holder AM, Breman AM, Dagli A, Bacino C, Scaglia F, Zori RT, Cheung SW, Scott DA, Kang SH. Wat MJ, et al. Among authors: cheung sw. Am J Med Genet A. 2009 Aug;149A(8):1661-77. doi: 10.1002/ajmg.a.32896. Am J Med Genet A. 2009. PMID: 19606479 Free PMC article.

6

OEIS complex associated with chromosome 1p36 deletion: a case report and review.

El-Hattab AW, Skorupski JC, Hsieh MH, Breman AM, Patel A, Cheung SW, Craigen WJ. El-Hattab AW, et al. Among authors: cheung sw. Am J Med Genet A. 2010 Feb;152A(2):504-11. doi: 10.1002/ajmg.a.33226. Am J Med Genet A. 2010. PMID: 20101692 Free article.

7

Delineation of a 1.65 Mb critical region for hemihyperplasia and digital anomalies on Xq25.

Ricks CB, Masand R, Fang P, Roney EK, Cheung SW, Scott DA. Ricks CB, et al. Among authors: cheung sw. Am J Med Genet A. 2010 Feb;152A(2):453-8. doi: 10.1002/ajmg.a.33227. Am J Med Genet A. 2010. PMID: 20101693

8

Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results.

Kang SH, Shaw C, Ou Z, Eng PA, Cooper ML, Pursley AN, Sahoo T, Bacino CA, Chinault AC, Stankiewicz P, Patel A, Lupski JR, Cheung SW. Kang SH, et al. Among authors: cheung sw. Am J Med Genet A. 2010 May;152A(5):1111-26. doi: 10.1002/ajmg.a.33278. Am J Med Genet A. 2010. PMID: 20340098 Free PMC article.

9

Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo events.

Bi W, Probst FJ, Wiszniewska J, Plunkett K, Roney EK, Carter BS, Williams MD, Stankiewicz P, Patel A, Stevens CA, Lupski JR, Cheung SW. Bi W, et al. Among authors: cheung sw. J Med Genet. 2012 Nov;49(11):681-8. doi: 10.1136/jmedgenet-2012-101002. Epub 2012 Oct 5. J Med Genet. 2012. PMID: 23042811

10

Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.

Lennon PA, Cooper ML, Curtis MA, Lim C, Ou Z, Patel A, Cheung SW, Bacino CA. Lennon PA, et al. Among authors: cheung sw. Am J Med Genet A. 2006 Jun 1;140(11):1156-63. doi: 10.1002/ajmg.a.31243. Am J Med Genet A. 2006. PMID: 16688748

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