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Archives Francaises De Pediatrie|March 1, 1980
[Osteomesopycnosis. A new autosomal dominant osteosclerosing bone disease (author's transl)]P MaroteauxHuman Genetics|May 1, 1989
Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive formP MaroteauxPediatric Research|October 1, 1975
Gel electrophoretic studies on proteoglycans and collagen of abnormal human growth cartilage: proteoglycan abnormalities in pseudoachondroplasia and in Kniest's diseaseV Stanescu, P MaroteauxAnnales De Pediatrie|May 1, 1993
[Type II primordial microcephalic dwarfism. Report of a patient with completed growth]D Théau, P MaroteauxArchives Francaises De Pediatrie|February 1, 1990
[Sublethal microcephalic chondrodysplasia. Taybi-Linder syndrome, primordial microcephalic nanism types I and III]P Maroteaux, J BadoualArchives Francaises De Pediatrie|February 1, 1988
[Hypochondroplasia. Review of 80 cases]P Maroteaux, P FalzonArchives Francaises De Pediatrie|December 1, 1977
[Study of the classification of chondrodysplasias with mesomelic predominance]P Maroteaux, J SprangerPediatric Radiology|January 1, 1991
The spondylometaphyseal dysplasias. A tentative classificationP Maroteaux, J SprangerArchives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1995
[Isolated bilateral dysplasia of the hip in children]C Vincent-Delorme, P MaroteauxPageof 42