Carey JC - Search Results

1

A dyadic approach to the delineation of diagnostic entities in clinical genomics.

Biesecker LG, Adam MP, Alkuraya FS, Amemiya AR, Bamshad MJ, Beck AE, Bennett JT, Bird LM, Carey JC, Chung B, Clark RD, Cox TC, Curry C, Dinulos MBP, Dobyns WB, Giampietro PF, Girisha KM, Glass IA, Graham JM Jr, Gripp KW, Haldeman-Englert CR, Hall BD, Innes AM, Kalish JM, Keppler-Noreuil KM, Kosaki K, Kozel BA, Mirzaa GM, Mulvihill JJ, Nowaczyk MJM, Pagon RA, Retterer K, Rope AF, Sanchez-Lara PA, Seaver LH, Shieh JT, Slavotinek AM, Sobering AK, Stevens CA, Stevenson DA, Tan TY, Tan WH, Tsai AC, Weaver DD, Williams MS, Zackai E, Zarate YA. Biesecker LG, et al. Among authors: carey jc. Am J Hum Genet. 2021 Jan 7;108(1):8-15. doi: 10.1016/j.ajhg.2020.11.013. Am J Hum Genet. 2021. PMID: 33417889 Free PMC article. Review.

2

The Coffin-Siris syndrome: five new cases including two siblings.

Carey JC, Hall BD. Carey JC, et al. Am J Dis Child. 1978 Jul;132(7):667-71. doi: 10.1001/archpedi.1978.02120320027005. Am J Dis Child. 1978. PMID: 665592

3

Confirmation of the Cohen syndrome.

Carey JC, Hall BD. Carey JC, et al. J Pediatr. 1978 Aug;93(2):239-44. doi: 10.1016/s0022-3476(78)80504-6. J Pediatr. 1978. PMID: 671157

4

Craniofacial malformations and their syndromes. An overview for the speech and hearing practitioner.

Carey JC, Stevens CA, Haskins R. Carey JC, et al. Clin Commun Disord. 1992 Fall;2(4):59-72. Clin Commun Disord. 1992. PMID: 1301906 Review.

5

Rubinstein-Taybi syndrome: a natural history study.

Stevens CA, Carey JC, Blackburn BL. Stevens CA, et al. Among authors: carey jc. Am J Med Genet Suppl. 1990;6:30-7. doi: 10.1002/ajmg.1320370605. Am J Med Genet Suppl. 1990. PMID: 2118775

6

Di George anomaly and velocardiofacial syndrome.

Stevens CA, Carey JC, Shigeoka AO. Stevens CA, et al. Among authors: carey jc. Pediatrics. 1990 Apr;85(4):526-30. Pediatrics. 1990. PMID: 2314965

7

Development of human palmar and digital flexion creases.

Stevens CA, Carey JC, Shah M, Bagley GP. Stevens CA, et al. Among authors: carey jc. J Pediatr. 1988 Jul;113(1 Pt 1):128-32. doi: 10.1016/s0022-3476(88)80546-8. J Pediatr. 1988. PMID: 3385521

8

Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.

Curry CJ, Carey JC, Holland JS, Chopra D, Fineman R, Golabi M, Sherman S, Pagon RA, Allanson J, Shulman S, et al. Curry CJ, et al. Among authors: carey jc. Am J Med Genet. 1987 Jan;26(1):45-57. doi: 10.1002/ajmg.1320260110. Am J Med Genet. 1987. PMID: 3812577

9

Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

Lowery MC, Morris CA, Ewart A, Brothman LJ, Zhu XL, Leonard CO, Carey JC, Keating M, Brothman AR. Lowery MC, et al. Among authors: carey jc. Am J Hum Genet. 1995 Jul;57(1):49-53. Am J Hum Genet. 1995. PMID: 7611295 Free PMC article.

10

Pulmonary hyperplasia in the Fraser cryptophthalmos syndrome.

Stevens CA, McClanahan C, Steck A, Shiel FO, Carey JC. Stevens CA, et al. Among authors: carey jc. Am J Med Genet. 1994 Oct 1;52(4):427-31. doi: 10.1002/ajmg.1320520407. Am J Med Genet. 1994. PMID: 7747754

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