Cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/5201093.pdf
Reference18 articles.
1. Shastry BS, Hiraoka M : Molecular genetics of familial exudative vitreoretinopathy and Norrie disease. Curr Genomics 2000; 1: 259–269.
2. Van Nouhuys CE : Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina. Doc Ophthalmol 1982; 54: 1–414.
3. Plager DA, Orgel IK, Ellis FD, Hartzer MK, Trese MT, Shastry BS : X-linked recessive familial exudative vitreoretinopathy. Am J Ophthalmol 1992; 114: 145–148.
4. Fullwood P, Jones J, Bundey S, Dudgeon J, Fielder AR, Kilpatric MW : X-linked exudative vitreoretinopathy: clinical features and genetic linkage analysis. Br J Ophthalmol 1993; 77: 168–170.
5. Shastry BS, Trese MT : Familial exudative vitreoretinopathy: further evidence for genetic heterogeneity. Am J Med Genet 1997; 69: 217–218.
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