Authors: Dollfus, H Kumaramanickavel, G Biswas, P Stoetzel, C Quillet, R Denton, M Maw, M Perrin-Schmitt, F

Citation: H. Dollfus et al., Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22, J MED GENET, 38(7), 2001, pp. 470-471

Authors: Maw, MA Corbeil, D Koch, J Hellwig, A Wilson-Wheeler, JC Bridges, RJ Kumaramanickavel, G John, S Nancarrow, D Roper, K Weigmann, A Huttner, WB Denton, MJ

Citation: Ma. Maw et al., A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration, HUM MOL GEN, 9(1), 2000, pp. 27-34

Authors: Gu, SM Kumaramanickavel, G Srikumari, CR Denton, MJ Gal, A

Citation: Sm. Gu et al., Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S 1337 and D2S286 on chromosome 2p11-p15 in an Indian family, J MED GENET, 36(9), 1999, pp. 705-707