These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
165 related articles for article (PubMed ID: 10544980)
21. Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. Wu WC; Drenser K; Trese M; Capone A; Dailey W Arch Ophthalmol; 2007 Feb; 125(2):225-30. PubMed ID: 17296899 [TBL] [Abstract][Full Text] [Related]
22. Differential diagnosis of Norrie disease and X-linked familial exudative vitreoretinopathy (XL-FEVR) based on clinical and molecular evaluation. Wawrocka A; Niedziela Z; Skorczyk-Werner A; Krawczynski MR Klin Oczna; 2016; 118(3):231-4. PubMed ID: 30088388 [TBL] [Abstract][Full Text] [Related]
23. X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis. Fullwood P; Jones J; Bundey S; Dudgeon J; Fielder AR; Kilpatrick MW Br J Ophthalmol; 1993 Mar; 77(3):168-70. PubMed ID: 8457509 [TBL] [Abstract][Full Text] [Related]
24. Lack of association of the Norrie disease gene with retinoschisis phenotype. Shastry BS; Hiraoka M; Trese MT Jpn J Ophthalmol; 2000; 44(6):627-9. PubMed ID: 11094177 [TBL] [Abstract][Full Text] [Related]
25. Evaluation of the norrie disease gene in a family with incontinentia pigmenti. Shastry BS; Trese MT Ophthalmic Res; 2000; 32(4):181-4. PubMed ID: 10828739 [TBL] [Abstract][Full Text] [Related]
26. Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy. Fuchs S; Kellner U; Wedemann H; Gal A Hum Mutat; 1995; 6(3):257-9. PubMed ID: 8535448 [No Abstract] [Full Text] [Related]
27. Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis. Black GC; Perveen R; Bonshek R; Cahill M; Clayton-Smith J; Lloyd IC; McLeod D Hum Mol Genet; 1999 Oct; 8(11):2031-5. PubMed ID: 10484772 [TBL] [Abstract][Full Text] [Related]
28. Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie disease. Yang H; Li S; Xiao X; Guo X; Zhang Q Curr Eye Res; 2012 Aug; 37(8):726-9. PubMed ID: 22563645 [TBL] [Abstract][Full Text] [Related]
29. [Analysis of the NDP gene in a Chinese family with X-linked recessive Norrie disease]. Mei L; Huang Y; Pan Q; Liang D; Wu L Zhonghua Yan Ke Za Zhi; 2015 May; 51(5):360-3. PubMed ID: 26311697 [TBL] [Abstract][Full Text] [Related]
30. [A literature review of Norrie disease]. Ohba N; Isashiki Y Nippon Ganka Gakkai Zasshi; 1996 Feb; 100(2):101-10. PubMed ID: 8851148 [TBL] [Abstract][Full Text] [Related]
31. Molecular dissection of Norrie disease. Berger W Acta Anat (Basel); 1998; 162(2-3):95-100. PubMed ID: 9831755 [TBL] [Abstract][Full Text] [Related]
32. Familial cases of Norrie disease detected by copy number analysis. Arai E; Fujimaki T; Yanagawa A; Fujiki K; Yokoyama T; Okumura A; Shimizu T; Murakami A Jpn J Ophthalmol; 2014 Sep; 58(5):448-54. PubMed ID: 25023092 [TBL] [Abstract][Full Text] [Related]
33. Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation. Khan AO; Aldahmesh MA; Meyer B Ophthalmology; 2008 Apr; 115(4):730-3. PubMed ID: 18387409 [TBL] [Abstract][Full Text] [Related]
34. Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease. Gal A; Wieringa B; Smeets DF; Bleeker-Wagemakers L; Ropers HH Cytogenet Cell Genet; 1986; 42(4):219-24. PubMed ID: 3502689 [TBL] [Abstract][Full Text] [Related]
35. Mutations in the candidate gene for Norrie disease. Berger W; van de Pol D; Warburg M; Gal A; Bleeker-Wagemakers L; de Silva H; Meindl A; Meitinger T; Cremers F; Ropers HH Hum Mol Genet; 1992 Oct; 1(7):461-5. PubMed ID: 1307245 [TBL] [Abstract][Full Text] [Related]
36. A novel c.287G>T Lin M; Lu Y; Sui Y; Ni X; Li H; Chen X; Zhao N; Jiang M Ophthalmic Genet; 2020 Aug; 41(4):338-340. PubMed ID: 32393149 [TBL] [Abstract][Full Text] [Related]
37. X-linked recessive primary retinal dysplasia is linked to the Norrie disease locus. Ravia Y; Braier-Goldstein O; Bat-Miriam KM; Erlich S; Barkai G; Goldman B Hum Mol Genet; 1993 Aug; 2(8):1295-7. PubMed ID: 8401512 [TBL] [Abstract][Full Text] [Related]
38. A novel mutation in the Norrie disease gene. Ott S; Patel RJ; Appukuttan B; Wang X; Stout JT J AAPOS; 2000 Apr; 4(2):125-6. PubMed ID: 10773814 [TBL] [Abstract][Full Text] [Related]
39. Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR). Toomes C; Downey LM; Bottomley HM; Scott S; Woodruff G; Trembath RC; Inglehearn CF Mol Vis; 2004 Jan; 10():37-42. PubMed ID: 14737064 [TBL] [Abstract][Full Text] [Related]