Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8

Author:

Blanton Susan Halloran,Heckenlively John R.,Cottingham Anne W.,Friedman Jackie,Sadler Lori A.,Wagner Michael,Friedman Lorraine H.,Daiger Stephen P.

Publisher

Elsevier BV

Subject

Genetics

Reference74 articles.

1. Dominant retinitis pigmentosa with reduced penetrance;Berson;Arch. Ophthalmol,1969

2. Dominant retinitis pigmentosa with reduced penetrance: further studies of the electroretinogram;Berson;Arch. Ophthalmol,1979

3. Identification of novel rhodopsin mutations in patients with autosomal dominant retinitis pigmentosa;Bhattacharya;Invest. Ophthalmol. Visual Sci,1991

4. Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q;Blanton;Genomics,1990

5. Exclusion map of type II autosomal dominant retinitis pigmentosa (ADRP);Blanton;Am. J. Hum. Genet,1990

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