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American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.La Nouvelle Presse Medicale|January 24, 1976
[Poland's syndrome. Clinical and genetic studies; physiopathologic considerations]J P Bouvet, P Maroteaux, M L Briard-GuillemotArchives Francaises De Pediatrie|April 1, 1986
[Antenatal forms of osteogenesis imperfecta. Classification trial]P Maroteaux, J Frézal, L Cohen-Solal, et al.Human Genetics|August 1, 1992
A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfectaJ Bonaventure, L Cohen-Solal, C Lasselin, et al.The Journal of Heredity|November 1, 1981
Fragilitas ossium: a new autosomal recessive mutation in the mouseJ L Guenet, R Stanescu, P Maroteaux, et al.American Journal of Medical Genetics|February 15, 1993
Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilageR Stanescu, V Stanescu, M P Muriel, et al.Archives Francaises De Pediatrie|October 1, 1975
[Pure spondylar dysplasia or brachyolmy. Apropos of a case]G Fontaine, P Maroteaux, J P Farriaux, et al.American Journal of Medical Genetics|March 1, 1989
OmodysplasiaP Maroteaux, J Sauvegrain, A Chrispin, et al.Annales De Genetique|January 1, 1990
Pseudodiastrophic dysplasia evolution with age and management. Report of two new cases and review of the literatureN Canki-Klain, V Stanescu, P Bebler, et al.Chirurgie Pediatrique|January 1, 1980
[Osteoarticular deformities in pseudo-achondroplastic dysplasia]G Finidori, P Rigault, P Maroteaux, et al.Pageof 29