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American Journal of Medical Genetics|March 1, 1988
Facial midline defect in the fetal alcohol syndrome: embryogenetic considerations in two clinical casesG Neri, V Sammito, C Romano, et al.
American Journal of Medical Genetics|August 3, 2001
Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18G Chamyan, D Debich-Spicer, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1985
Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from MontanaJ M Opitz, R B Lowry, T M Holmes, et al.
European Journal of Pediatrics|March 18, 1977
A biologic and genetic study of 40 cases of severe pure mental retardationJ M Becker, E G Kaveggia, E Pendleton, et al.
European Journal of Pediatrics|February 21, 1977
Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?G Neuhäuser, G M ZuRhein, E G Kaveggia, et al.
American Journal of Medical Genetics. Part A|October 30, 2013
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988G Neri, R Marini, M Cappa, et al.
European Journal of Pediatrics|July 1, 1977
Studies of malformation syndromes of man XLVII: disappearance of spermatogonia in the Fanconi anemia syndromeG J Bargman, N T Shahidi, E F Gilbert, 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.
American Journal of Medical Genetics|October 1, 1987
Sudden death in childhood in a case of the G syndromeS L Einfeld, M J Fairley, B F Green, et al.
European Journal of Pediatrics|February 21, 1977
Hemihypotrophy in a girl with a translocation t(13q;7p)F A Marçallo, L C Werneck, R F Pilotto, et al.
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