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Annales De Genetique|January 1, 1992
Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe "boomerang dysplasia"?N Canki-Klain, V Stanescu, R Stanescu, 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.Archives Francaises De Pediatrie|December 1, 1978
[Fibrochondrogenesis]F Lazzaroni-Fossati, V Stanescu, R Stanescu, et al.Annales De Genetique|January 1, 1985
Incontinentia pigmenti (IP) and r(X). Tentative mapping of the IP locus to the X juxtacentromeric regionJ de Grouchy, C Turleau, M Doussau de Bazignan, et al.American Journal of Medical Genetics|August 22, 1997
Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineationA Loshkajian, J Roume, V Stanescu, et al.Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|January 1, 1990
[Multiple pterygium syndrome in children. 7 cases]B Fenoll, P Rigault, P Maroteaux, et al.Journal Francais D'Ophtalmologie|January 1, 1980
[Ocular findings in a peculiar type of mucolipidosis called nephrosialidosis]J L Dufier, P Dhermy, S Limon, 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 25, 1998
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndromeM Bahuau, C Houdayer, B Assouline, et al.Pageof 29