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.
179 related articles for article (PubMed ID: 8573024)
1. Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21. Héon E; Piguet B; Munier F; Sneed SR; Morgan CM; Forni S; Pescia G; Schorderet D; Taylor CM; Streb LM; Wiles CD; Nishimura DY; Sheffield VC; Stone EM Arch Ophthalmol; 1996 Feb; 114(2):193-8. PubMed ID: 8573024 [TBL] [Abstract][Full Text] [Related]
2. Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen. Edwards AO; Klein ML; Berselli CB; Hejtmancik JF; Rust K; Wirtz MK; Weleber RG; Acott TS Am J Ophthalmol; 1998 Sep; 126(3):417-24. PubMed ID: 9744375 [TBL] [Abstract][Full Text] [Related]
3. The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16. Gregory CY; Evans K; Wijesuriya SD; Kermani S; Jay MR; Plant C; Cox N; Bird AC; Bhattacharya SS Hum Mol Genet; 1996 Jul; 5(7):1055-9. PubMed ID: 8817347 [TBL] [Abstract][Full Text] [Related]
4. A new locus for dominant drusen and macular degeneration maps to chromosome 6q14. Kniazeva M; Traboulsi EI; Yu Z; Stefko ST; Gorin MB; Shugart YY; O'Connell JR; Blaschak CJ; Cutting G; Han M; Zhang K Am J Ophthalmol; 2000 Aug; 130(2):197-202. PubMed ID: 11004294 [TBL] [Abstract][Full Text] [Related]
5. Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration. Stefko ST; Zhang K; Gorin MB; Traboulsi EI Am J Ophthalmol; 2000 Aug; 130(2):203-8. PubMed ID: 11004295 [TBL] [Abstract][Full Text] [Related]
6. Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. Klein ML; Schultz DW; Edwards A; Matise TC; Rust K; Berselli CB; Trzupek K; Weleber RG; Ott J; Wirtz MK; Acott TS Arch Ophthalmol; 1998 Aug; 116(8):1082-8. PubMed ID: 9715689 [TBL] [Abstract][Full Text] [Related]
7. Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration. Guymer RH; McNeil R; Cain M; Tomlin B; Allen PJ; Dip CL; Baird PN Clin Exp Ophthalmol; 2002 Dec; 30(6):419-23. PubMed ID: 12427233 [TBL] [Abstract][Full Text] [Related]
8. An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5. Michaelides M; Johnson S; Tekriwal AK; Holder GE; Bellmann C; Kinning E; Woodruff G; Trembath RC; Hunt DM; Moore AT Invest Ophthalmol Vis Sci; 2003 May; 44(5):2178-83. PubMed ID: 12714659 [TBL] [Abstract][Full Text] [Related]
9. Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q. Stone EM; Nichols BE; Kimura AE; Weingeist TA; Drack A; Sheffield VC Arch Ophthalmol; 1994 Jun; 112(6):765-72. PubMed ID: 8002834 [TBL] [Abstract][Full Text] [Related]
10. Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy. Evans K; Gregory CY; Wijesuriya SD; Kermani S; Jay MR; Plant C; Bird AC Arch Ophthalmol; 1997 Jul; 115(7):904-10. PubMed ID: 9230832 [TBL] [Abstract][Full Text] [Related]
11. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1). Brown J; Fingert JH; Taylor CM; Lake M; Sheffield VC; Stone EM Arch Ophthalmol; 1997 Jan; 115(1):95-9. PubMed ID: 9006432 [TBL] [Abstract][Full Text] [Related]
15. Molecular genetic heterogeneity in autosomal dominant drusen. Tarttelin EE; Gregory-Evans CY; Bird AC; Weleber RG; Klein ML; Blackburn J; Gregory-Evans K J Med Genet; 2001 Jun; 38(6):381-4. PubMed ID: 11389162 [TBL] [Abstract][Full Text] [Related]
16. Mapping of autosomal dominant cone degeneration to chromosome 17p. Small KW; Syrquin M; Mullen L; Gehrs K Am J Ophthalmol; 1996 Jan; 121(1):13-8. PubMed ID: 8554076 [TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian family. Lagali PS; MacDonald IM; Griesinger IB; Chambers ML; Ayyagari R; Wong PW Can J Ophthalmol; 2000 Oct; 35(6):315-24. PubMed ID: 11091913 [TBL] [Abstract][Full Text] [Related]
18. Dominant radial drusen and Arg345Trp EFEMP1 mutation. Matsumoto M; Traboulsi EI Am J Ophthalmol; 2001 Jun; 131(6):810-2. PubMed ID: 11384588 [TBL] [Abstract][Full Text] [Related]
19. A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Stone EM; Lotery AJ; Munier FL; Héon E; Piguet B; Guymer RH; Vandenburgh K; Cousin P; Nishimura D; Swiderski RE; Silvestri G; Mackey DA; Hageman GS; Bird AC; Sheffield VC; Schorderet DF Nat Genet; 1999 Jun; 22(2):199-202. PubMed ID: 10369267 [TBL] [Abstract][Full Text] [Related]
20. A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family. Yang Z; Kitsos G; Tong Z; Payne M; Gorezis S; Psilas K; Grigoriadou M; Zhao Y; Kamaya S; Aperis G; Petersen MB; Zhang K J Med Genet; 2006 Dec; 43(12):e57. PubMed ID: 17142619 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]