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Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.Clinical Orthopaedics and Related Research|January 1, 1976
The lethal chondrodysplasiasP Maroteaux, V Stanescu, R StanescuThe Journal of Bone and Joint Surgery. American Volume|July 1, 1984
Pathogenic mechanisms in osteochondrodysplasiasV Stanescu, R Stanescu, P MaroteauxAnnales De Genetique|January 1, 1987
[Cloverleaf skull associated with generalized bone defects close to asphyxiating thoracic dysplasia]A Benallègue, F Lacete, P MaroteauxHuman 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 MaroteauxPageof 29