Title: Familial exudative vitreoretinopathy: Further evidence for genetic heterogeneity
Abstract: American Journal of Medical GeneticsVolume 69, Issue 2 p. 217-218 Letter to the Editor Familial exudative vitreoretinopathy: Further evidence for genetic heterogeneity Barkur S. Shastry, Corresponding Author Barkur S. Shastry Eye Research Institute, Oakland University, Rochester, MichiganEye Research Institute, Oakland University, Rochester, MI 48309-4401Search for more papers by this authorMichael T. Trese, Michael T. Trese Department of Ophthalmology, William Beaumont Hospital, Royal Oak, MichiganSearch for more papers by this author Barkur S. Shastry, Corresponding Author Barkur S. Shastry Eye Research Institute, Oakland University, Rochester, MichiganEye Research Institute, Oakland University, Rochester, MI 48309-4401Search for more papers by this authorMichael T. Trese, Michael T. Trese Department of Ophthalmology, William Beaumont Hospital, Royal Oak, MichiganSearch for more papers by this author First published: 06 December 1998 https://doi.org/10.1002/(SICI)1096-8628(19970317)69:2<217::AID-AJMG19>3.0.CO;2-OCitations: 32AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References Chen Z-Y, Bettinelli EM, Fielder A, Bundey S, Sims K, Breakfield SO, Craig IW: (1993): A mutation in the Norrie disease gene associated with X-linked familial exudative vitreoretinopathy. Nature Genet 5: 180–182. Clement F, Beckford CA, Corral A, Jimenez R (1995): X-linked familial exudative vitreoretinopathy. Retina 15: 141–145. Criswick VG, Schepens CL (1969): Familial exudative vitreoretinopathy. Am J Ophthalmol 68: 578–594. Fuchs S, Kellner U, Wedemann H, Gal A (1995): Missense mutation in the Norrie disease gene associated with X-linked exudative vitreoretinopathy. Hum Mutat 6: 257–259. Fullwood P, Jones J, Bundey S, Dudgeon J, Fielder AR, Kilpatric MW (1993): X-linked exudative vitreoretinopathy: Clinical features and genetic linkage analysis. Br J Ophthalmol 77: 168–170. Li Y, Muller B, Fuhrmann C, Van Nouhuys CE, Laqua H, Humphries P, Schwinger E, Gal A (1992): The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11533. Am J Hum Genet 51: 749–754. Plager DA, Orgel IK, Ellis FD, Hartzer MK, Trese MT, Shastry BS (1992): X-linked recessive familial exudative vitreoretinopathy. Am J Ophthalmol 114: 145–148. Shastry BS, Hejtmancik JF, Plager DA, Hartzer MK, Trese MT (1995): Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy. Genomics 27: 341–344. Van Nouhuys CE (1982): Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina. Doc Ophthalmol 54: 1–414. Warburg M (1971): Norrie disease. Birth Defects 7: 117–124. Citing Literature Volume69, Issue217 March 1997Pages 217-218 ReferencesRelatedInformation
Publication Year: 1997
Publication Date: 1997-03-17
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 43
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