Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

Author:

Aldred M A,Teague P W,Jay M,Bundey S,Redmond R M,Jay B,Bird A C,Bhattacharya S S,Wright A F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. On the heredity of retinitis pigmentosa;Jay, M.;Br J Ophthalmol,1982

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

3. Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests;Ott, J.; Bhattacharya, S.; Chen, J.D.;Proc Nad Acad Sci USA,1990

4. Localisation of the gene for X linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis;Musarella, M.A.; Burghes, A.; Anson-Cartwright, L.;Am J Hum Genet,1988

5. Multipoint linkage analysis and heterogeneity testing in 20 X linked retinitis pigmentosa families;Musarella, M.A.; Anson-Cartwright, L.; Leal, S.M.;Genomics,1990

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