The annual incidence of DiGeorge/velocardiofacial syndrome.

Author:

Devriendt K,Fryns J P,Mortier G,van Thienen M N,Keymolen K

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference19 articles.

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

2. Rhodopsin mutations in autosomal dominant retinitis pigmentosa;Sung, C.H.; Davenport, C.M.; Hennessey, J.C.;Proc Natl Acad Sci USA,1991

3. A genetic survey of twenty dominant retinitis pigmentosa families: frequencies of the eight known loci and evidence for further heterogeneity;Inglehearn, C.F.; Tarttelin, E.E.; Plant, C.;J Med Genet,1998

4. A ninth locus (RP18) for autosomal dominant retinitis transmission is known. minimum estimate, since many cases with mild features remain undiagnosed. In the pigmentosa maps in the pericentric region of chromosome 1;Xu, S.; Schwartz, M.; Rosenberg, T.; Gal, A.;Hum Mol Genet,1996

5. A clinical, psychophysical and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa;Lyness, A.L.; Ernst, W.; Quinlan, M.P.,1985

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