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: Rodrigues, NR Theodosiou, AM Nesbit, MA Campbell, L Tandle, AT Saranath, D Davies, KE

Citation: Nr. Rodrigues et al., Characterization of Ngef, a novel member of the Dbl family of genes expressed predominantly in the caudate nucleus, GENOMICS, 65(1), 2000, pp. 53-61

Authors: Van Esch, H Groenen, P Nesbit, MA Schuffenhauer, S Lichtner, P Vanderlinden, G Harding, B Beetz, R Bilous, RW Holdaway, I Shaw, NJ Fryns, JP Van de Ven, WV Thakker, RV Devriendt, K

Citation: H. Van Esch et al., GATA3 haplo-insufficiency causes human HDR syndrome, NATURE, 406(6794), 2000, pp. 419-422