Carey JC - Search Results

1

Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.

Sung SS, Brassington AM, Grannatt K, Rutherford A, Whitby FG, Krakowiak PA, Jorde LB, Carey JC, Bamshad M. Sung SS, et al. Among authors: carey jc. Am J Hum Genet. 2003 Mar;72(3):681-90. doi: 10.1086/368294. Am J Hum Genet. 2003. PMID: 12592607 Free PMC article.

2

Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers.

Ward K, O'Connell P, Carey JC, Leppert M, Jolley S, Plaetke R, Ogden B, White R. Ward K, et al. Among authors: carey jc. Am J Hum Genet. 1990 May;46(5):943-9. Am J Hum Genet. 1990. PMID: 1971145 Free PMC article.

3

Precise localization of NF1 to 17q11.2 by balanced translocation.

Ledbetter DH, Rich DC, O'Connell P, Leppert M, Carey JC. Ledbetter DH, et al. Among authors: carey jc. Am J Hum Genet. 1989 Jan;44(1):20-4. Am J Hum Genet. 1989. PMID: 2491776 Free PMC article.

4

Prenatal diagnosis of distal arthrogryposis.

Baty BJ, Cubberley D, Morris C, Carey J. Baty BJ, et al. Am J Med Genet. 1988 Mar;29(3):501-10. doi: 10.1002/ajmg.1320290305. Am J Med Genet. 1988. PMID: 3287922 Review.

5

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

6

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.

7

A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.

Bamshad M, Watkins WS, Zenger RK, Bohnsack JF, Carey JC, Otterud B, Krakowiak PA, Robertson M, Jorde LB. Bamshad M, et al. Among authors: carey jc. Am J Hum Genet. 1994 Dec;55(6):1153-8. Am J Hum Genet. 1994. PMID: 7977374 Free PMC article.

8

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

9

Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.

Hales HA, Peterson CM, Carey J, Hecht BK, Hecht F. Hales HA, et al. Am J Med Genet. 1993 Nov 1;47(6):848-51. doi: 10.1002/ajmg.1320470610. Am J Med Genet. 1993. PMID: 8279482 Review.

10

A gene for ulnar-mammary syndrome maps to 12q23-q24.1.

Bamshad M, Krakowiak PA, Watkins WS, Root S, Carey JC, Jorde LB. Bamshad M, et al. Among authors: carey jc. Hum Mol Genet. 1995 Oct;4(10):1973-7. doi: 10.1093/hmg/4.10.1973. Hum Mol Genet. 1995. PMID: 8595424

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

409 results

Search Page

Filters