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Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15.
Cheung SW, Shaffer LG, Richards CS, Page SL, Riconda DL. Cheung SW, et al. Am J Med Genet. 1997 Oct 3;72(1):47-50. doi: 10.1002/(sici)1096-8628(19971003)72:1<47::aid-ajmg10>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9295074
Confirmation of paternal disomy in a twin molar pregnancy. A case report.
Kirshon B, Reiter A, Adam K, Cheung SW. Kirshon B, et al. Among authors: cheung sw. J Reprod Med. 2000 Jan;45(1):39-41. J Reprod Med. 2000. PMID: 10664946
The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3.
Stankiewicz P, Cheung SW, Shaw CJ, Saleki R, Szigeti K, Lupski JR. Stankiewicz P, et al. Among authors: cheung sw. Cytogenet Genome Res. 2003;101(2):118-23. doi: 10.1159/000074166. Cytogenet Genome Res. 2003. PMID: 14610351
Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.
Yatsenko SA, Yatsenko AN, Szigeti K, Craigen WJ, Stankiewicz P, Cheung SW, Lupski JR. Yatsenko SA, et al. Among authors: cheung sw. Clin Genet. 2004 Aug;66(2):128-36. doi: 10.1111/j.1399-0004.2004.00290.x. Clin Genet. 2004. PMID: 15253763
Congenital diaphragmatic hernia in WAGR syndrome.
Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW. Scott DA, et al. Among authors: cheung sw. Am J Med Genet A. 2005 May 1;134(4):430-3. doi: 10.1002/ajmg.a.30654. Am J Med Genet A. 2005. PMID: 15779010 Review.
Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly.
Yatsenko SA, Cheung SW, Scott DA, Nowaczyk MJ, Tarnopolsky M, Naidu S, Bibat G, Patel A, Leroy JG, Scaglia F, Stankiewicz P, Lupski JR. Yatsenko SA, et al. Among authors: cheung sw. J Med Genet. 2005 Apr;42(4):328-35. doi: 10.1136/jmg.2004.028258. J Med Genet. 2005. PMID: 15805160 Free PMC article. No abstract available.
Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
Hwang KS, Pearson MA, Stankiewicz P, Lennon PA, Cooper ML, Wu J, Ou Z, Cai WW, Patel A, Cheung SW. Hwang KS, et al. Among authors: cheung sw. Am J Med Genet A. 2005 Aug 15;137(1):88-93. doi: 10.1002/ajmg.a.30858. Am J Med Genet A. 2005. PMID: 16015583
Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Cheung SW, Shaw CA, Yu W, Li J, Ou Z, Patel A, Yatsenko SA, Cooper ML, Furman P, Stankiewicz P, Lupski JR, Chinault AC, Beaudet AL. Cheung SW, et al. Genet Med. 2005 Jul-Aug;7(6):422-32. doi: 10.1097/01.gim.0000170992.63691.32. Genet Med. 2005. PMID: 16024975
Prenatal diagnosis of PLP1 copy number by array comparative genomic hybridization.
Lee JA, Cheung SW, Ward PA, Inoue K, Lupski JR. Lee JA, et al. Among authors: cheung sw. Prenat Diagn. 2005 Dec;25(13):1188-91. doi: 10.1002/pd.1308. Prenat Diagn. 2005. PMID: 16353282
WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
Lennon PA, Scott DA, Lonsdorf D, Wargowski DS, Kirkpatrick S, Patel A, Cheung SW. Lennon PA, et al. Among authors: cheung sw. Am J Med Genet A. 2006 Jun 1;140(11):1214-8. doi: 10.1002/ajmg.a.31229. Am J Med Genet A. 2006. PMID: 16646034
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