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.
3. 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]
4. An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4. Michaelides M; Johnson S; Poulson A; Bradshaw K; Bellmann C; Hunt DM; Moore AT Invest Ophthalmol Vis Sci; 2003 Apr; 44(4):1657-62. PubMed ID: 12657606 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. The benign concentric annular macular dystrophy locus maps to 6p12.3-q16. van Lith-Verhoeven JJ; Hoyng CB; van den Helm B; Deutman AF; Brink HM; Kemperman MH; de Jong WH; Kremer H; Cremers FP Invest Ophthalmol Vis Sci; 2004 Jan; 45(1):30-5. PubMed ID: 14691150 [TBL] [Abstract][Full Text] [Related]
10. A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus. Rabb MF; Mullen L; Yelchits S; Udar N; Small KW Am J Ophthalmol; 1998 Apr; 125(4):502-8. PubMed ID: 9559736 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss. Francis PJ; Johnson S; Edmunds B; Kelsell RE; Sheridan E; Garrett C; Holder GE; Hunt DM; Moore AT Br J Ophthalmol; 2003 Jul; 87(7):893-8. PubMed ID: 12812894 [TBL] [Abstract][Full Text] [Related]
13. Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14. Edwards AO; Miedziak A; Vrabec T; Verhoeven J; Acott TS; Weleber RG; Donoso LA Am J Ophthalmol; 1999 Apr; 127(4):426-35. PubMed ID: 10218695 [TBL] [Abstract][Full Text] [Related]
14. Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy. Mansergh FC; Kenna PF; Rudolph G; Meitinger T; Farrar GJ; Kumar-Singh R; Scorer J; Hally AM; Mynett-Johnson L; Humphries MM J Med Genet; 1995 Nov; 32(11):855-8. PubMed ID: 8592326 [TBL] [Abstract][Full Text] [Related]
15. North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2. Small KW; Weber J; Roses A; Pericak-Vance P Ophthalmic Paediatr Genet; 1993 Dec; 14(4):143-50. PubMed ID: 8015785 [TBL] [Abstract][Full Text] [Related]
16. Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids. Graff C; Eriksson A; Forsman K; Sandgren O; Holmgren G; Wadelius C Hum Genet; 1997 Dec; 101(3):263-70. PubMed ID: 9439653 [TBL] [Abstract][Full Text] [Related]
17. North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis. Small KW Trans Am Ophthalmol Soc; 1998; 96():925-61. PubMed ID: 10360311 [TBL] [Abstract][Full Text] [Related]
18. North Carolina macular dystrophy (MCDR1) in Texas. Small KW; Garcia CA; Gallardo G; Udar N; Yelchits S Retina; 1998; 18(5):448-52. PubMed ID: 9801042 [TBL] [Abstract][Full Text] [Related]