Authors: Kelly, AL Lunt, PW Rodrigues, F Berry, PJ Flynn, DM McKiernan, PJ Kelly, DA Mieli-Vergani, G Cox, TM

Citation: Al. Kelly et al., Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in ironmetabolism, J MED GENET, 38(9), 2001, pp. 599-610

Authors: Lunt, PW

Citation: Pw. Lunt, Facioscapulohumeral muscular dystrophy: Diagnostic and molecular aspects, MG CLIN NEU, 18, 2000, pp. 44-60

Authors: Stalker, DJ Vigneswaren, S Sharples, PM Lunt, PW

Citation: Dj. Stalker et al., Distal trisomy 2p and arachnodactyly, J MED GENET, 37(12), 2000, pp. 974-976

Authors: Schweiger, S Foerster, J Lehman, T Suckow, V Muller, YA Walter, G Davies, T Porter, H van Bokhoven, H Lunt, PW Traub, P Ropers, HH

Citation: S. Schweiger et al., The Opitz syndrome gene product, MID1, associates with microtubules, P NAS US, 96(6), 1999, pp. 2794-2799

Authors: Cantlay, AM Shokrollahi, K Allen, JT Lunt, PW Newbury-Ecob, RA Steward, CG

Citation: Am. Cantlay et al., Genetic analysis of the G4.5 gene in families with suspected Barth syndrome, J PEDIAT, 135(3), 1999, pp. 311-315

Authors: Inglehearn, CF McHale, JC Keen, TJ Skirton, H Lunt, PW

Citation: Cf. Inglehearn et al., A new family linked to the RP1 dominant retinitis pigmentosa locus on chromosome 8q, J MED GENET, 36(8), 1999, pp. 646-648