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Human Genetics|July 1, 1995
Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasiasJ Bonaventure, F Chaminade, P MaroteauxArchives Francaises De Pediatrie|April 1, 1984
[Dyssegmental dysplasia. Apropos of 2 familial cases with fatal development]M Bueno, J Argemi, P MaroteauxAnnales De Biologie Clinique|January 1, 1985
[Cellular aspects of chondrodysplasia]V Stanescu, R Stanescu, P MaroteauxAmerican Journal of Medical Genetics|February 15, 1993
DysspondylochondromatosisP Freisinger, G Finidori, P MaroteauxArchives Francaises De Pediatrie|March 1, 1984
[Spondyloepiphyseal dysplasia with an accumulation of glycoproteins in chondrocytes]R Stanescu, V Stanescu, P MaroteauxAnnales De Biologie Clinique|January 1, 1986
[The genetics of collagen diseases]J Kaplan, P Maroteaux, J FrezalJournal De Radiologie|December 1, 1981
[Roentgenological evolution of bone maturation. A case of congenital myxoedema treated at forty years old (author's transl)]R Leclercq, P Maroteaux, M BardLa Nouvelle Presse Medicale|November 1, 1975
[Ultrastructural abnormalities of the chondrocytes in pycnodysostosis. Their relation to a disorder of lipid metabolism]R Stanescu, V Stanescu, P MaroteauxAnnales De Genetique|January 1, 1986
Congenital absence of the tibiae and thumbs with polydactyly. A rare genetic disease (Werner's syndrome)I Cordeiro, H Santos, P MaroteauxBiochimica Et Biophysica Acta|May 7, 1980
Proteoglycan populations of baboon (Papio papio) cartilages from different anatomical sites: gel electrophoretic analysis of dissociated proteoglycans and of fractions obtained by density gradient centrifugationV Stanescu, P Maroteaux, E SobczakPageof 42