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Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
South ST, Whitby H, Maxwell T, Aston E, Brothman AR, Carey JC. South ST, et al. Among authors: carey jc. Am J Med Genet A. 2008 Oct 15;146A(20):2691-7. doi: 10.1002/ajmg.a.32516. Am J Med Genet A. 2008. PMID: 18798325
Survival in trisomy 18.
Root S, Carey JC. Root S, et al. Among authors: carey jc. Am J Med Genet. 1994 Jan 15;49(2):170-4. doi: 10.1002/ajmg.1320490203. Am J Med Genet. 1994. PMID: 8116664
Cytogenetic and molecular analysis in trisomy 12p.
Allen TL, Brothman AR, Carey JC, Chance PF. Allen TL, et al. Among authors: carey jc. Am J Med Genet. 1996 May 3;63(1):250-6. doi: 10.1002/(SICI)1096-8628(19960503)63:1<250::AID-AJMG43>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8723118 Review.
409 results