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The Journal of Clinical Investigation|February 12, 1998
Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13M J Econs, P T McEnery, F Lennon, et al.Genomics|July 1, 1990
The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets geneM J Econs, M A Pericak-Vance, H Betz, et al.The Journal of Clinical Endocrinology and Metabolism|July 1, 1992
Multilocus mapping of the X-linked hypophosphatemic rickets geneM J Econs, D F Barker, M C Speer, et al.Bone|July 28, 1999
New insights into the pathogenesis of inherited phosphate wasting disordersM J EconsThe American Journal of Physiology|November 15, 1997
Positional cloning of the PEX gene: new insights into the pathophysiology of X-linked hypophosphatemic ricketsM J Econs, F FrancisAmerican Journal of Medical Genetics|June 22, 2000
Heterogeneity in Paget disease of the boneM A Nance, F Q Nuttall, M J Econs, et al.Somatic Cell and Molecular Genetics|October 20, 1998
Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3K E White, M J EconsThe Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorderM J Econs, P T McEneryJournal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.Pageof 12