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Human Genetics|July 1, 1991
Dominant mutations in familial lethal and severe osteogenesis imperfectaL Cohen-Solal, J Bonaventure, P MaroteauxArchives 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.Journal of Medical Genetics|July 1, 1992
Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndromeJ Bonaventure, C Lasselin, J Mellier, et al.Biochimica Et Biophysica Acta|October 31, 1986
Abnormal procollagen synthesis in fibroblasts from three patients of the same family with a severe form of osteogenesis imperfecta (type III)J Bonaventure, L Cohen-Solal, C Lasselin, et al.Connective Tissue Research|January 1, 1985
Age related evolution of stable collagen reticulation in human skinM Le Lous, L Cohen-Solal, J C Allain, et al.Connective Tissue Research|January 1, 1989
Localization of gamma-glutamyl-phosphate residues to the alpha 2CB3-5 peptide of type I chicken bone collagenJ C Landais, L Cohen-Solal, J Bonaventure, et al.American Journal of Medical Genetics|February 15, 1994
Achondrogenesis type IB (Fraccaro): study of collagen in the tissue and in chondrocytes cultured in agaroseP Freisinger, V Stanescu, B Jacob, et al.Annales De Genetique|January 1, 1984
[Lethal osteogenesis imperfecta. Definition and heterogeneity]P Maroteaux, L Cohen-SolalAmerican Journal of Medical Genetics|July 1, 1989
A new lethal brittle bone syndrome with increased amount of type V collagen in a patientJ Bonaventure, L Zylberberg, L Cohen-Solal, et al.Pageof 24