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American Journal of Medical Genetics|April 24, 1996
Revised diagnostic criteria for the Marfan syndromeA De Paepe, R B Devereux, H C Dietz, et al.American Journal of Medical Genetics|May 3, 1996
Diastrophic dysplasia: extreme variability within a sibshipB D HallAmerican Journal of Medical Genetics|May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasiaB F Pontz, H Stöss, F Henschke, et al.American Journal of Medical Genetics|May 3, 1996
Osteopathia striata with cranial sclerosis: variable expressivity in a four generation pedigreeR König, C Dukiet, A Dörries, et al.American Journal of Medical Genetics|May 3, 1996
An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short statureH Menger, S Mundlos, K Becker, et al.American Journal of Medical Genetics|May 3, 1996
Molecular defects in the chondrodysplasiasD L RimoinAmerican Journal of Medical Genetics|May 3, 1996
Phenotypic expressions of a Gly 154Arg mutation in type II collagen in two unrelated patients with spondyloepimetaphyseal dysplasia (SEMD)I Kaitila, J Körkkö, E Marttinen, et al.American Journal of Medical Genetics|May 3, 1996
Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfismJ Bonaventure, F Rousseau, L Legeai-Mallet, et al.American Journal of Medical Genetics|May 3, 1996
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfectaK M Dyne, M Valli, A Forlino, et al.American Journal of Medical Genetics|May 3, 1996
Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?E Majewski, T Goecke, P MeineckePageof 854