Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.

Author:

Mansergh F C,Kenna P F,Rudolph G,Meitinger T,Farrar G J,Kumar-Singh R,Scorer J,Hally A M,Mynett-Johnson L,Humphries M M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. UJber eine hereditare Maculaaffektion: Beitrage zur Vererbungslehre;Best, R.Z.,1905

2. New clinical test of retinal function based on the standing potential of the eye;Arden, G.B.; Barrada, A.; Kelsey, J.H.;Br J Ophthalmol,1962

3. Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 1 1ql3;Stone, E.M.; Nichols, B.E.; Streb, L.M.; Kimura, A.E.; Sheffield, V.C.;Nature Genet,1992

4. The gene for Best's macular dystrophy is located at 11 qi 3 in a Swedish family;Forsman, K.; Graff, C.; Nordstrom, S.;Clin Genet,1992

5. High resolution meiotic and physical mapping of the Best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11;Weber, B.H.; Vogt, G.; Stohr, H.; Sander, S.; Walker, D.; Jones, C.;Am Hum Genet,1994

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