Authors: Inglehearn, C. F. Bashir, R. Lester, D. H. Jay, M. Bird, A. C. Bhattacharya, S. S.

Citation: F. Inglehearn, C. et al., A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa., American journal of human genetics , 48-I(1), 1991, pp. 26-30

Authors: Lester, D. H. Inglehearn, C. F. Bashir, R. Ackford, H. Esakowitz, L. Jay, M. Bird, A. C. Wright, A. F. Papiha, S. S. Bhattacharya, S. S.

Citation: H. Lester, D. et al., Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity., American journal of human genetics , 47-I(3), 1990, pp. 536-541

Authors: Farrar, G. J. Kenna, P. Redmond, R. McWilliam, P. Bradley, D.G. Humphries, M. M Sharp, E.M. Inglehearn, C. F. Bashir, R. Jay, M. Watty, A. Ludwig, M. Schinzel, A. Samanns, C. Gal, A. Bhattacharya, S. Humphries, P.

Citation: J. Farrar, G. et al., Autosomal dominant retinitis pigmentosa: Absence of the rhodopsin proline.histidine substitution (codon 23) in pedigrees from Europe, American journal of human genetics , 47-II(6), 1990, pp. 941-945