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: Bibb, LC Holt, JKL Tarttelin, EE Hodges, MD Gregory-Evans, K Rutherford, A Lucas, RJ Sowden, JC Gregory-Evans, CY

Citation: Lc. Bibb et al., Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development., HUM MOL GEN, 10(15), 2001, pp. 1571-1579

Authors: Tarttelin, EE Gregory-Evans, CY Bird, AC Weleber, RG Klein, ML Blackburn, J Gregory-Evans, K

Citation: Ee. Tarttelin et al., Molecular genetic heterogeneity in autosomal dominant drusen, J MED GENET, 38(6), 2001, pp. 381-384

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: Kermani, S Gregory-Evans, K Tarttelin, EE Bellingham, J Plant, C Bird, AC Fox, M Bhattacharya, SS Gregory-Evans, CY

Citation: S. Kermani et al., Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD), HUM GENET, 104(1), 1999, pp. 77-82

Authors: Tarttelin, EE Kirschner, LS Bellingham, J Baffi, J Taymans, SE Gregory-Evans, K Csaky, K Stratakis, CA Gregory-Evans, CY

Citation: Ee. Tarttelin et al., Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16, BIOC BIOP R, 260(1), 1999, pp. 174-180