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American Journal of Medical Genetics|November 1, 1984
Acrofacial dysplasia resembling geleophysic dysplasiaJ Spranger, E F Gilbert, S Flatz, et al.
European Journal of Pediatrics|April 1, 1990
Mental retardation syndrome with renal concentration deficiency and intracerebral calcificationO Schofer, R Beetz, J Bohl, et al.
Human Mutation|January 1, 1994
Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutationA Winterpacht, M Hilbert, U Schwarze, et al.
American Journal of Medical Genetics|January 15, 1993
Osteogenesis imperfecta and hyperplastic callus formation: light- and electron-microscopic findingsH Stöss, B Pontz, U Vetter, 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|August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest diseaseL O Langer, M Gonzalez-Ramos, H Chen, et al.
Pediatric Radiology|January 1, 1982
Congenital generalized fibromatosis. Case report and literature reviewP W Brill, D R Yandow, L O Langer, et al.
American Journal of Human Genetics|March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasiaM Deere, S H Blanton, C I Scott, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics|November 1, 1984
Geleophysic dysplasiaJ Spranger, E F Gilbert, S Arya, et al.
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