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American Journal of Human Genetics|October 23, 1997
Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndromeS B Bleyl, B R Mumford, V Thompson, et al.Journal of Musculoskeletal & Neuronal Interactions|June 14, 2005
Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomographyD A Stevenson, L J Moyer-Mileur, J C Carey, et al.American Journal of Human Genetics|February 1, 1997
A variant of Freeman-Sheldon syndrome maps to 11p15.5-pterP A Krakowiak, J R O'Quinn, J F Bohnsack, et al.American Journal of Medical Genetics|August 15, 2001
Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogeneticsZ Chen, A Meloni-Ehrig, J C Palumbos, et al.American Journal of Ophthalmology|September 15, 1984
Congenital corneal opacification secondary to Bowman's layer dysgenesisD J Apple, R J Olson, G R Jones, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|August 1, 1996
Children and adolescents with neurofibromatosis 1: a behavioral phenotypeC V Dilts, J C Carey, J C Kircher, et al.The Journal of Infectious Diseases|June 1, 1995
The genital flora of women with intraamniotic infection. Vaginal Infection and Prematurity Study GroupM A Krohn, S L Hillier, R P Nugent, et al.American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.American Journal of Medical Genetics|March 31, 1997
Six patients with oral-facial-digital syndrome IV: the case for heterogeneityH V Toriello, J C Carey, E Suslak, et al.American Journal of Medical Genetics|November 14, 2000
Growth failure, intracranial calcifications, acquired pancytopenia, and unusual humoral immunodeficiency: a genetic syndrome?E E Adderson, D H Viskochil, J C Carey, et al.Pageof 16