Carey JC - Search Results

1

Three novel GJB2 (connexin 26) variants associated with autosomal dominant syndromic and nonsyndromic hearing loss.

DeMille D, Carlston CM, Tam OH, Palumbos JC, Stalker HJ, Mao R, Zori RT, Viskochil DH, Park AH, Carey JC. DeMille D, et al. Among authors: carey jc. Am J Med Genet A. 2018 Apr;176(4):945-950. doi: 10.1002/ajmg.a.38648. Am J Med Genet A. 2018. PMID: 29575629

2

Nosological considerations of the neurofibromatoses.

Viskochil D, Carey JC. Viskochil D, et al. Among authors: carey jc. J Dermatol. 1992 Nov;19(11):873-80. doi: 10.1111/j.1346-8138.1992.tb03798.x. J Dermatol. 1992. PMID: 1293176

3

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, Culver M, Carey JC, Copeland NG, Jenkins NA, et al. Viskochil D, et al. Among authors: carey jc. Cell. 1990 Jul 13;62(1):187-92. doi: 10.1016/0092-8674(90)90252-a. Cell. 1990. PMID: 1694727

4

The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene.

Viskochil D, Cawthon R, O'Connell P, Xu GF, Stevens J, Culver M, Carey J, White R. Viskochil D, et al. Mol Cell Biol. 1991 Feb;11(2):906-12. doi: 10.1128/mcb.11.2.906-912.1991. Mol Cell Biol. 1991. PMID: 1899288 Free PMC article.

5

The NF1 translocation breakpoint region.

O'Connell P, Cawthon RM, Viskochil D, White R, Carey JC, Buchberg AM. O'Connell P, et al. Among authors: carey jc. Ann N Y Acad Sci. 1991;615:319-31. doi: 10.1111/j.1749-6632.1991.tb37774.x. Ann N Y Acad Sci. 1991. PMID: 1903909 Review.

6

Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindred.

Viskochil DH, Carey JC, Glader BE, Rothstein G, Christensen RD. Viskochil DH, et al. Among authors: carey jc. Am J Med Genet. 1990 Feb;35(2):251-6. doi: 10.1002/ajmg.1320350221. Am J Med Genet. 1990. PMID: 2309764

7

Delineation of the male phenotype in carniofrontonasal syndrome.

Morris CA, Palumbos JC, Carey JC. Morris CA, et al. Among authors: carey jc. Am J Med Genet. 1987 Jul;27(3):623-31. doi: 10.1002/ajmg.1320270315. Am J Med Genet. 1987. PMID: 3631134

8

Familial total anomalous pulmonary venous return: a large Utah-Idaho family.

Bleyl S, Ruttenberg HD, Carey JC, Ward K. Bleyl S, et al. Among authors: carey jc. Am J Med Genet. 1994 Oct 1;52(4):462-6. doi: 10.1002/ajmg.1320520412. Am J Med Genet. 1994. PMID: 7747759

9

Current status of the human malformation map.

Carey JC, Viskochil DH. Carey JC, et al. Birth Defects Orig Artic Ser. 1996;30(1):13-34. Birth Defects Orig Artic Ser. 1996. PMID: 9125323 Review.

10

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

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