6 results for author:"Oudet C.L." in Literature citations
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| MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia. Rowe P.S.N., de Zoysa P.A., Dong R., Wang H.R., White K.E., Econs M.J., Oudet C.L. Genomics 67:54-68(2000) · UniProtKB (1) |
| Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues. Filisetti D., Ostermann G., von Bredow M., Strom T.M., Filler G., Ehrich J., Pannetier S., Garnier J.-M., Rowe P.S.N., Francis F. et al. Eur. J. Hum. Genet. 7:615-619(1999) · UniProtKB (1) |
| A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets. Econs M.J., Friedman N.E., Rowe P.S.N., Speer M.C., Francis F., Strom T.M., Oudet C.L., Smith J.A., Ninomiya J.T., Lee B.E. et al. J. Clin. Endocrinol. Metab. 83:3459-3462(1998) · UniProtKB (1) |
| Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets. Francis F., Strom T.M., Hennig S., Boeddrich A., Lorenz B., Brandau O., Mohnike K.L., Cagnoli M., Steffens C., Klages S. et al. |
| Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP). Rowe P.S.N., Oudet C.L., Francis F., Sinding C., Pannetier S., Econs M.J., Strom T.M., Meitinger T., Garabedian M., David A. et al. Hum. Mol. Genet. 6:539-549(1997) · UniProtKB (1) |
| A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP consortium |