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Birth Defects Research. Part A, Clinical and Molecular Teratology|June 12, 2003
Specific congenital heart defects in RSH/Smith-Lemli-Opitz syndrome: postulated involvement of the sonic hedgehog pathway in syndromes with postaxial polydactyly or heterotaxiaMaria Cristina Digilio, Bruno Marino, Aldo Giannotti, et al.Fetal and Pediatric Pathology|February 15, 2012
Premature closure of the foramen ovale secondary to congenital aortic valvular stenosis in a stillbornLarissa V Furtado, Angelica R Putnam, Lance K Erickson, et al.American Journal of Medical Genetics|November 1, 1985
NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndromeA Daniel, L Ekblom, S Phillips, et al.European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesisE T Bersu, J C Pettersen, W J Charboneau, et al.American Journal of Medical Genetics|February 1, 1982
Phenotypic effects of inherited balanced translocationZ Ying, C Zaiyu, L Chunyun, et al.American Journal of Medical Genetics. Part A|January 7, 2009
Elements of morphology: standard terminology for the periorbital regionBryan D Hall, John M Graham, Suzanne B Cassidy, et al.American Journal of Medical Genetics. Part A|October 30, 2013
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. 1984Giovanni Neri, Maria Enrica Martini-Neri, Ben E Katz, et al.American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.American Journal of Medical Genetics|January 1, 1979
The Johanson-Blizzard syndrome: case report and autopsy findingsD L Daentl, J L Frías, E F Gilbert, et al.Pageof 34