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American Journal of Ophthalmology|February 1, 1980
The cerebro-oculo-facio-skeletal syndromeW S Grizzard, J J O'Donnell, J C CareyPediatric Pathology|January 1, 1989
Pulmonary hypoplasia in mice homozygous for the cartilage matrix deficiency (cmd) gene: a model for human congenital disorderM J Houghton, J C Carey, R E SeegmillerAmerican Journal of Medical Genetics. Part A|December 15, 2005
Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysisA Battaglia, A Novelli, C Ceccarini, et al.American Journal of Medical Genetics|February 15, 1993
Brachymesomelia and Peters anomaly: a new syndromeJ D Kivlin, J C Carey, M A RicheyAmerican Journal of Medical Genetics|January 15, 1994
Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence riskB J Baty, B L Blackburn, J C CareyPediatrics|April 1, 1990
Di George anomaly and velocardiofacial syndromeC A Stevens, J C Carey, A O ShigeokaInternational Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|April 6, 1999
Prior third- or fourth-degree perineal tears and recurrence risksT N Payne, J C Carey, W F RayburnAmerican Journal of Medical Genetics|July 1, 1993
Acalvaria: a unique congenital anomalyC P Harris, J J Townsend, J C CareyAmerican Journal of Medical Genetics|July 3, 1995
Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation familyK K Norton, J C Carey, D H GutmannThe Journal of Pediatrics|November 1, 1982
The Robin sequence as a consequence of malformation, dysplasia, and neuromuscular syndromesJ C Carey, R M Fineman, F A ZiterPageof 16