Authors: Suri, M Brueton, LA Venkatraman, N Cox, PM

Citation: M. Suri et al., MURCS association with encephalocele: report of a second case, CLIN DYSMOR, 9(1), 2000, pp. 31-33

Authors: Brueton, LA Huson, SM Cox, PM Shirley, I Thompson, EM Barnes, PRJ Price, J Newsom-Davis, J Vincent, A

Citation: La. Brueton et al., Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype, AM J MED G, 92(1), 2000, pp. 1-6

Authors: Brady, AF Waters, CS Pocha, MJ Brueton, LA

Citation: Af. Brady et al., Chronic myelomonocytic leukaemia in a child with constitutional partial trisomy 8 mosaicism, CLIN GENET, 58(2), 2000, pp. 142-146

Authors: Goodman, FR Bacchelli, C Brady, AF Brueton, LA Fryns, JP Mortlock, DP Innis, JW Holmes, LB Donnenfeld, AE Feingold, M Beemer, FA Hennekam, RCM Scambler, PJ

Citation: Fr. Goodman et al., Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome, AM J HU GEN, 67(1), 2000, pp. 197-202

Authors: Cox, PM Brueton, LA Murphy, KW Worthington, VC Bjelogrlic, P Lazda, EJ Sabire, NJ Sewry, CA

Citation: Pm. Cox et al., Early-onset fetal hydrops and muscle degeneration in siblings due to a novel variant of type IV glycogenosis, AM J MED G, 86(2), 1999, pp. 187-193