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American Journal of Medical Genetics|December 1, 1984
The Potter sequence: a clinical analysis of 80 casesC J Curry, K Jensen, J Holland, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1981
Deletion mapping of sequences essential for in vivo transcription of the iso-1-cytochrome c geneG Faye, D W Leung, K Tatchell, et al.
The Journal of Pediatrics|September 1, 1975
Macrocephaly in association with unusual cutaneous angiomatosisM J Stephan, B D Hall, D W Smith, et al.
The Journal of Bone and Joint Surgery. American Volume|July 1, 1985
Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a familyJ P Drawbert, D B Stevens, R G Cadle, et al.
American Journal of Human Genetics|January 1, 1989
Precise localization of NF1 to 17q11.2 by balanced translocationD H Ledbetter, D C Rich, P O'Connell, et al.
Clinical Dysmorphology|January 29, 2000
Wolf-Hirschhorn syndrome (WHS): a history in picturesA Battaglia, J C Carey, D H Viskochil, et al.
American Journal of Medical Genetics|February 5, 1998
Variegated aneuploidy in two siblings: phenotype, genotype, CENP-E analysis, and literature reviewW L Flejter, B Issa, B A Sullivan, et al.
Estuaries and Coasts : Journal of the Estuarine Research Federation|October 2, 2018
Anthropocene survival of southern New England's salt marshesE B Watson, K B Raposa, J C Carey, et al.
AJR. American Journal of Roentgenology|April 1, 1997
Large vestibular aqueduct syndrome: a genetic disease?K A Tong, H R Harnsberger, R T Dahlen, et al.
The Journal of Pediatrics|June 1, 1983
Femoral hypoplasia-unusual facies syndrome in infants of diabetic mothersJ P Johnson, J C Carey, W M Gooch, et al.
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