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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.Southern Medical Journal|March 1, 1979
Malignant transformation of polyostotic fibrous dysplasiaC B Johnson, E F Gilbert, L I GottliebArchives of Pathology & Laboratory Medicine|July 1, 1977
Uhl's anomaly in the mink. Partial absence of the right atrial and ventricular myocardiumS Ishikawa, G M Zu Rhein, E F GilbertArchives of Pathology & Laboratory Medicine|June 1, 1983
Menkes' syndrome with vascular and adrenergic nerve abnormalitiesH Uno, S Arya, R Laxova, et al.Archives of Pathology & Laboratory Medicine|March 1, 1979
Angiosarcoma of the spleen: a report of two cases and review of the literatureK T Chen, J C Bolles, E F GilbertCancer|August 1, 1975
Prognostic features of thyroid cancer. A long-term followup of 68 casesM A Russell, E F Gilbert, W F JaeschkeTeratology|October 1, 1983
External malformations in chick embryos following concomitant administration of methylxanthines and beta-adrenomimetic agents: 1. Gross pathologic featuresH J Bruyere, J F Fallon, E F GilbertPageof 57