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.
126 related articles for article (PubMed ID: 15851557)
1. No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy. Yellore VS; Rayner SA; Emmert-Buck L; Tabin GC; Raber I; Hannush SB; Stulting RD; Sampat K; Momi R; Principe AH; Aldave AJ Invest Ophthalmol Vis Sci; 2005 May; 46(5):1599-603. PubMed ID: 15851557 [TBL] [Abstract][Full Text] [Related]
2. No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy. Aldave AJ; Rayner SA; Salem AK; Yoo GL; Kim BT; Saeedian M; Sonmez B; Yellore VS Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3787-90. PubMed ID: 16936088 [TBL] [Abstract][Full Text] [Related]
3. Keratoconus is not associated with mutations in COL8A1 and COL8A2. Aldave AJ; Bourla N; Yellore VS; Rayner SA; Khan MA; Salem AK; Sonmez B Cornea; 2007 Sep; 26(8):963-5. PubMed ID: 17721297 [TBL] [Abstract][Full Text] [Related]
16. Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus. Abd El-Aziz MM; El-Ashry MF; Barragan I; Marcos I; Borrego S; Antiñolo G; Bhattacharya SS Curr Eye Res; 2005 Dec; 30(12):1081-7. PubMed ID: 16354621 [TBL] [Abstract][Full Text] [Related]
17. A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene. Aldave AJ; Rayner SA; King JA; Affeldt JA; Yellore VS Ophthalmology; 2005 Jun; 112(6):1017-22. PubMed ID: 15885785 [TBL] [Abstract][Full Text] [Related]
18. Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy. Yellore VS; Khan MA; Bourla N; Rayner SA; Chen MC; Sonmez B; Momi RS; Sampat KM; Gorin MB; Aldave AJ Mol Vis; 2007 Sep; 13():1777-82. PubMed ID: 17960116 [TBL] [Abstract][Full Text] [Related]
19. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
20. TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients. Chakravarthi SV; Kannabiran C; Sridhar MS; Vemuganti GK Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):121-5. PubMed ID: 15623763 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]