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Health supervision and anticipatory guidance of individuals with Wolf-Hirschhorn syndrome.
Battaglia A, Carey JC. Battaglia A, et al. Among authors: carey jc. Am J Med Genet. 1999 Jun 25;89(2):111-5. doi: 10.1002/(sici)1096-8628(19990625)89:2<111::aid-ajmg9>3.0.co;2-g. Am J Med Genet. 1999. PMID: 10559766 Review.
New syndrome involving the visual, auditory, respiratory, gastrointestinal, and renal systems.
Siegler RL, Brewer ED, Carey JC. Siegler RL, et al. Among authors: carey jc. Am J Med Genet. 1992 Nov 1;44(4):461-4. doi: 10.1002/ajmg.1320440415. Am J Med Genet. 1992. PMID: 1442888
Health supervision and anticipatory guidance for children with genetic disorders (including specific recommendations for trisomy 21, trisomy 18, and neurofibromatosis I).
Carey JC. Carey JC. Pediatr Clin North Am. 1992 Feb;39(1):25-53. doi: 10.1016/s0031-3955(16)38261-x. Pediatr Clin North Am. 1992. PMID: 1531255
Three diagnostic signs in Williams syndrome.
Morris CA, Carey JC. Morris CA, et al. Among authors: carey jc. Am J Med Genet Suppl. 1990;6:100-1. doi: 10.1002/ajmg.1320370618. Am J Med Genet Suppl. 1990. PMID: 2118769
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
Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.
Schwartz CE, Johnson JP, Holycross B, Mandeville TM, Sears TS, Graul EA, Carey JC, Schroer RJ, Phelan MC, Szollar J, et al. Schwartz CE, et al. Among authors: carey jc. Am J Hum Genet. 1988 Nov;43(5):597-604. Am J Hum Genet. 1988. PMID: 2903661 Free PMC article.
Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
Toriello HV, Carey JC. Toriello HV, et al. Among authors: carey jc. Am J Med Genet. 1988 Sep;31(1):17-23. doi: 10.1002/ajmg.1320310105. Am J Med Genet. 1988. PMID: 3223497
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
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
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.
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