A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.

Author:

Inglehearn C F,Tarttelin E E,Plant C,Peacock R E,al-Maghtheh M,Vithana E,Bird A C,Bhattacharya S S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. Population genetic studies of retinitis pigmentosa;Boughman, J.A.; Conneally, P.M.; Nance, W.E.;Am J Hum Genet,1980

2. Prevalence of retinitis pigmentosa in Maine;Bunker, C.H.; Berson, E.L.; Bromley, W.C.; Hayes, R.P.; Roderick, T.H.;Am J Ophthalmol,1984

3. Retinal photoreceptor dystrophies. Edward Jackson Memorial Lecture;Bird, A.C.;Am J Ophthalmol,1995

4. A study of retinitis pigmentosa in the city of Birmingham. II. Clinical and genetic heterogeneity;Bundey, S.; Crews, S.J.;J7 Med Genet,1984

5. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentric region of chromosome 1;Xu, S.Y.; Schwartz, M.; Rosenburg, T.; Gal, A.;Hum Mol Genet,1996

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