Authors: Bell, R Brice, G Child, AH Murday, VA Mansour, S Sandy, CJ Collin, JRO Brady, AF Callen, DF Burnand, K Mortimer, P Jeffery, S

Citation: R. Bell et al., Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene, HUM GENET, 108(6), 2001, pp. 546-551

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: Brady, AF Elsawi, MM Jamieson, CR Marks, K Jeffery, S Patton, MA Murtaza, L Savage, MO

Citation: Af. Brady et al., Clinical and molecular findings in a patient with a deletion on the long arm of chromosome 12, J MED GENET, 36(12), 1999, pp. 939-941