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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.
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
American Journal of Medical Genetics|September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomaliesG Neri, M E Martini-Neri, B E Katz, et al.
Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.
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