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American Journal of Medical Genetics|December 18, 1996
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis associationM Bahuau, W Flintoff, B Assouline, et al.American Journal of Medical Genetics|August 17, 1999
Facial anomalies in D-2-hydroxyglutaric aciduriaJ Amiel, P de Lonlay, C Francannet, et al.Journal of Neurosurgery|March 6, 1999
Clinical variability in patients with Apert's syndromeE Lajeunie, R Cameron, V El Ghouzzi, et al.Archives Francaises De Pediatrie|August 1, 1984
[Acromesomelic dysplasia. Apropos of a new case]P Stichelbout, R Pratz, G Lemaitre, et al.American Journal of Medical Genetics|September 1, 1984
Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebraeP Maroteaux, V Stanescu, R Stanescu, et al.Journal of Medical Genetics|July 1, 1990
Microspherophakia-metaphyseal dysplasia: a 'new' dominantly inherited bone dysplasia with severe eye involvementA Verloes, L Van Maldergem, P de Marneffe, et al.Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.American Journal of Medical Genetics|October 12, 2002
Clinical and genetic heterogeneity of Seckel syndromeL Faivre, M Le Merrer, S Lyonnet, et al.American Journal of Medical Genetics|December 5, 2000
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeL Faivre, A M Prieur, M Le Merrer, et al.Archives Francaises De Pediatrie|December 1, 1978
[Culture of normal and pathological human growth cartilage. Action of vitamin D derivatives and somatomedin]M T Corvol, M F Dumontier, P Maroteaux, et al.Pageof 29