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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.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|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.American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.Pageof 19