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