Carey JC - Search Results

1

The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignancies.

Shen W, Heeley JM, Carlston CM, Acuna-Hidalgo R, Nillesen WM, Dent KM, Douglas GV, Levine KL, Bayrak-Toydemir P, Marcelis CL, Shinawi M, Carey JC. Shen W, et al. Among authors: carey jc. Am J Med Genet A. 2017 Nov;173(11):3022-3028. doi: 10.1002/ajmg.a.38485. Epub 2017 Sep 21. Am J Med Genet A. 2017. PMID: 28941052

2

Natural history of trisomy 18 and trisomy 13: II. Psychomotor development.

Baty BJ, Jorde LB, Blackburn BL, Carey JC. Baty BJ, et al. Among authors: carey jc. Am J Med Genet. 1994 Jan 15;49(2):189-94. doi: 10.1002/ajmg.1320490205. Am J Med Genet. 1994. PMID: 7509567

3

Multiple congenital anomalies in a man with (X;6) translocation.

Sivak LE, Esbenshade J, Brothman AR, Issa B, Lemons RS, Carey JC. Sivak LE, et al. Among authors: carey jc. Am J Med Genet. 1994 May 15;51(1):9-12. doi: 10.1002/ajmg.1320510103. Am J Med Genet. 1994. PMID: 8030680

4

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.

5

Distal arthrogryposis type 1: clinical analysis of a large kindred.

Bamshad M, Bohnsack JF, Jorde LB, Carey JC. Bamshad M, et al. Among authors: carey jc. Am J Med Genet. 1996 Nov 11;65(4):282-5. doi: 10.1002/(SICI)1096-8628(19961111)65:4<282::AID-AJMG7>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8923936

6

Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B).

Krakowiak PA, Bohnsack JF, Carey JC, Bamshad M. Krakowiak PA, et al. Among authors: carey jc. Am J Med Genet. 1998 Feb 26;76(1):93-8. doi: 10.1002/(sici)1096-8628(19980226)76:1<93::aid-ajmg17>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9508073

7

Microcephaly with simplified gyral pattern in six related children.

Peiffer A, Singh N, Leppert M, Dobyns WB, Carey JC. Peiffer A, et al. Among authors: carey jc. Am J Med Genet. 1999 May 21;84(2):137-44. doi: 10.1002/(sici)1096-8628(19990521)84:2<137::aid-ajmg10>3.0.co;2-j. Am J Med Genet. 1999. PMID: 10323739

8

Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogenetics.

Chen Z, Meloni-Ehrig A, Palumbos JC, Guan XY, Carroll KL, Dent KM, Carey JC. Chen Z, et al. Among authors: carey jc. Am J Med Genet. 2001 Sep 1;102(4):379-82. doi: 10.1002/ajmg.1470. Am J Med Genet. 2001. PMID: 11503167

9

Methodology of a multistate study of congenital hearing loss: preliminary data from Utah newborn screening.

Dent KM, Kenneson A, Palumbos JC, Maxwell S, Eichwald J, White K, Mao R, Bale JF Jr, Carey JC. Dent KM, et al. Among authors: carey jc. Am J Med Genet C Semin Med Genet. 2004 Feb 15;125C(1):28-34. doi: 10.1002/ajmg.c.30002. Am J Med Genet C Semin Med Genet. 2004. PMID: 14755431

10

6q subtelomeric deletion: is there a recognizable syndrome?

Stevenson DA, Brothman AR, Carey JC, Chen Z, Dent KM, Bale JF Jr, Longo N. Stevenson DA, et al. Among authors: carey jc. Clin Dysmorphol. 2004 Apr;13(2):103-106. Clin Dysmorphol. 2004. PMID: 15057127

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