X chromosome inactivation pattern in female carriers of X linked hypophosphataemic rickets.

Author:

Orstavik K H,Orstavik R E,Halse J,Knudtzon J

Publisher

BMJ

Reference13 articles.

1. Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2);Rowe, P.S.N.;Hum Genet,1994

2. The HYP Consortium. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphataemic rickets;Nature Genet,1995

3. X-linked hypophosphatemia: A homologous phenotype in humans and mice with unusual organ-specific gene dosage;Scriver, C.R.; Tenenhouse, H.S.;J7 Inherited Metab Dis,1992

4. A genetic study of familial hypophosphatemia and vitamin D resistant rickets with a review of the literature;Winters, R.W.; Graham, J.B.; Williams, T.F.; Burnett, McFalls V.W.; C.H.;Medicine,1958

5. Vitamin D-resistant rickets: analysis of twenty-four pedigrees with hereditary and sporadic cases;Burnett, C.H.; Dent, C.E.; Harper, C.; Warland, B.J.;Am Med,1964

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