Authors: McKie, AB McHale, JC Keen, TJ Tarttelin, EE Goliath, R van Lith-Verhoeven, JJC Greenberg, J Ramesar, RS Hoyng, CB Cremers, FPM Mackey, DA Bhattacharya, SS Bird, AC Markham, AF Inglehearn, CF

Citation: Ab. Mckie et al., Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominantretinitis pigmentosa (RP13), HUM MOL GEN, 10(15), 2001, pp. 1555-1562

Authors: Danciger, M Hendrickson, J Lyon, J Toomes, C McHale, JC Fishman, GA Inglehearn, CF Jacobson, SG Farber, DB

Citation: M. Danciger et al., CORD9 a new locus for arCRD: Mapping to 8p11, estimation of frequency, evaluation of a candidate gene, INV OPHTH V, 42(11), 2001, pp. 2458-2465

Authors: McHale, JC McKie, AB Tarttelin, EE Inglehearn, CF

Citation: Jc. Mchale et al., Expression map of human chromosome region 17p13.3, spanning the RP13 dominant retinitis pigmentosa locus, the Miller-Dieker lissencephaly syndrome (MDLS) region, and a putative tumour suppressor locus, CYTOG C GEN, 88(3-4), 2000, pp. 225-229

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