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Pathologie-Biologie|October 1, 1979
[A new method for extraction of cartilage proteoglycans: the electrical extraction (author's transl)]V Stanescu, R Stanescu, P MaroteauxAmerican Journal of Medical Genetics|August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndromeS Briault, S Odent, J Lucas, et al.Journal of Medical Genetics|July 4, 2001
Genotype-phenotype correlation in hereditary multiple exostosesC Francannet, A Cohen-Tanugi, M Le Merrer, et al.European Journal of Pediatrics|July 1, 1992
X-linked hydrocephalus: clinical heterogeneity at a single gene locusF Serville, S Lyonnet, A Pelet, et al.American Journal of Medical Genetics|August 15, 1994
Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndromeP Edery, Y Manach, M Le Merrer, et al.Human Genetics|August 1, 1996
Possible genetic heterogeneity in the Saethre-Chotzen syndromeH W Ma, E Lajeunie, N de Parseval, et al.Journal of Pediatric Orthopedics. Part B|January 1, 1997
Brachytelephalangic chondrodysplasia punctata in a female childM O Peter, E Jeandidier, P MaroteauxJournal of Medical Genetics|November 1, 1992
An atypical form of mucolipidosis IIIP Freisinger, J C Padovani, P MaroteauxLa Nouvelle Presse Medicale|September 20, 1975
[Poly-epiphyseal dysplasia, probably autosomal recessive. Contribution of the ultrastructural study to the discovery of this autonomous form]P Maroteaux, R Stanescu, D Cohen-SolalHuman Genetics|July 1, 1991
Dominant mutations in familial lethal and severe osteogenesis imperfectaL Cohen-Solal, J Bonaventure, P MaroteauxPageof 29