Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.-Reference-Cited by-同舟云学术

Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval.

Published:1995-03-01 Issue:3 Volume:32 Page:224-226
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Gregory C Y,Evans K,Bhattacharya S S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. A colour atlas of corneal dystrophies and degenerations;Casey, T.A.; Sharif, K.W.,1991

2. Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalised amyloidosis;Donder, P.C.; Blanksma, L.J.;Ophthalrnologica,1979

3. sons diseases of the cornea;Gray, Arffa R.C.,1991

4. Phenotypic variation in combined granular-lattice (Avellino) corneal dystrophy;Rosenwasser, G.O.D.; Sucheski, B.M.; Rosa, N.;Arch Ophthalniol,1993

5. Three etic heterogeneity, but phenotypic variation autosomal dominant comeal dystrophies map to chromosome 5q;Stone, E.M.; Mathers, W.D.; Rosenwasser, G.O.D.;Nature Genzet,1993

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