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Clinical Genetics|March 18, 2006
Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotypeD A Stevenson, D H Viskochil, A F Rope, et al.
American Journal of Medical Genetics|May 14, 1999
Microcephaly with simplified gyral pattern in six related childrenA Peiffer, N Singh, M Leppert, et al.
Pediatrics|May 1, 1984
Further delineation of the 10p deletion syndromeC L Elstner, J C Carey, G Livingston, et al.
American Journal of Medical Genetics|May 3, 1996
Cytogenetic and molecular analysis in trisomy 12pT L Allen, A R Brothman, J C Carey, et al.
American Journal of Medical Genetics|August 1, 1991
Osteochondrodysplasia with rhizomelia, platyspondyly, callosal agenesis, thrombocytopenia, hydrocephalus, and hypertensionO M Faye-Petersen, K Ward, J C Carey, et al.
The Journal of Reproductive Medicine|August 1, 1997
Midtrimester pregnancy termination for fetal malformations. Use of intravaginal prostaglandin E2D L Hagar, M T Valley, W F Rayburn, et al.
American Journal of Medical Genetics|January 15, 1994
Natural history of trisomy 18 and trisomy 13: II. Psychomotor developmentB J Baty, L B Jorde, B L Blackburn, et al.
Radiology|March 1, 1981
Short-limbed dwarfism: ultrasonographic diagnosis by mensuration of fetal femoral lengthR A Filly, M S Golbus, J C Carey, et al.
Pharmacology, Biochemistry, and Behavior|July 1, 1976
Behavioral depression: thyroid interactions with norepinephrine-depleting drugsJ W Davenport, R S Hennies, J C Carey, et al.
Teratology|June 1, 1986
Pulmonary hypoplasia in chondrodystrophic miceR E Seegmiller, C A Cooper, M J Houghton, et al.
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