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Results: 1-6 |
Results: 6

Authors: Christie, PT Harding, B Nesbit, MA Whyte, MP Thakker, RV
Citation: Pt. Christie et al., X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene, J CLIN END, 86(8), 2001, pp. 3840-3844

Authors: Christie, PT Curley, A Nesbit, MA Chapman, C Genet, S Harper, PS Keeling, SL Wilkie, AOM Winter, RM Thakker, RV
Citation: Pt. Christie et al., Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda, J CLIN END, 86(7), 2001, pp. 3233-3236

Authors: Yamamoto, K Cox, JPDT Friedrich, T Christie, PT Bald, M Houtman, PN Lapsley, MJ Patzer, L Tsimaratos, M Van't Hoff, WG Yamaoka, K Jentsch, TJ Thakker, RV
Citation: K. Yamamoto et al., Characterization of renal chloride channel (CLCN5) mutations in Dent's disease, J AM S NEPH, 11(8), 2000, pp. 1460-1468

Authors: Mumm, S Christie, PT Finnegan, P Jones, J Dixon, PH Pannett, AAJ Harding, B Gottesman, GS Thakker, RV Whyte, MP
Citation: S. Mumm et al., A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred, J CLIN END, 85(9), 2000, pp. 3343-3347

Authors: Devuyst, O Christie, PT Courtoy, PJ Beauwens, R Thakker, RV
Citation: O. Devuyst et al., Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease, HUM MOL GEN, 8(2), 1999, pp. 247-257

Authors: Cox, JPD Yamamoto, K Christie, PT Wooding, C Feest, T Flinter, FA Goodyer, PR Leumann, E Neuhaus, T Reid, C Williams, PF Wrong, O Thakker, RV
Citation: Jpd. Cox et al., Renal chloride channel, CLCN5, mutations in Dent's disease, J BONE MIN, 14(9), 1999, pp. 1536-1542
Risultati: 1-6 |