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