Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.

Author:

Field L L,Heckenlively J R,Sparkes R S,Garcia C A,Farson C,Zedalis D,Sparkes M C,Crist M,Tideman S,Spence M A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1977

2. Review, retinitis pigmentosa;Merin, M.D.; Auerbach, E.;Survey Ophthalmol,1976

3. Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1;Spence, M.A.; Sparkes, R.S.; Heckenlively, JR;Am J Hum Genet,1977

4. Spence MA, Sparkes RS, Heckenlively JR, et al. Erratum. Am J Hum Genet 1977;29:592.

5. A computer program for linkage analysis of general human pedigrees;Ott, J.;Am J Hum Genet; Age-of-onset available for linkage analysis (LIPED,1976

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