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American Journal of Medical Genetics|March 31, 1997
Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delayM Feingold, B D Hall, Y Lacassie, et al.
Teratology|March 15, 2000
Mini-review: history of organized teratology information services in North AmericaM Leen-Mitchell, L Martinez, S Gallegos, et al.
The EMBO Journal|January 1, 1982
Genetic analysis of the processing of a spliced tRNAK Nishikura, J Kurjan, B D Hall, et al.
American Journal of Medical Genetics|March 10, 2001
Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual developmentB J Baty, S B Olson, R E Magenis, et al.
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.
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