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Annales De Genetique|September 1, 1976
[Intracellular glycosaminoglycans of diploid and heteroploid human cells and of hybrid cell lines issued from their fusion]M C Hors-Cayla, S Heuertz, P MaroteauxArchives Francaises De Pediatrie|June 1, 1975
[Bone dysplasia with dwarfism and diffuse skeletal alterations]C Piussan, P Maroteaux, I Castroviejo, et al.The Journal of Rheumatology|October 1, 1987
Pathologic features of the femoral heads in a patient aged 14 1/2 years with spondyloepiphyseal dysplasia with osteoarthritisR Stanescu, V Stanescu, C Bordat, et al.Hormone Research|November 29, 2008
Pamidronate treatment of children with moderate-to-severe osteogenesis imperfecta: a note of cautionM Alharbi, G Pinto, G Finidori, et al.La Revue De Medecine Interne|August 7, 2002
[Hereditary multiple exostoses after 40 years of development: a case report]J Rambeloarisoa, M el Guedj, L Legeai-Mallet, et al.Nature Genetics|March 1, 1994
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locusP Saugier-Veber, A Munnich, D Bonneau, et al.Clinical Genetics|August 31, 1999
Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of diastrophic dysplasiaA Mégarbané, F A Haddad, S Haddad-Zebouni, et al.Journal of Medical Genetics|May 1, 1993
X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locusD Bonneau, J M Rozet, C Bulteau, et al.Mechanisms of Development|October 24, 1998
Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossificationA L Delezoide, C Benoist-Lasselin, L Legeai-Mallet, et al.Human Molecular Genetics|April 1, 1996
Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)F Rousseau, V el Ghouzzi, A L Delezoide, et al.Pageof 29