168 related articles for article (PubMed ID: 17976682)
1. Clinical characterization and genetic mapping of North Carolina macular dystrophy.
Yang Z; Tong Z; Chorich LJ; Pearson E; Yang X; Moore A; Hunt DM; Zhang K
Vision Res; 2008 Feb; 48(3):470-7. PubMed ID: 17976682
[TBL] [Abstract][Full Text] [Related]
2. An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1).
Sauer CG; Schworm HD; Ulbig M; Blankenagel A; Rohrschneider K; Pauleikhoff D; Grimm T; Weber BH
J Med Genet; 1997 Dec; 34(12):961-6. PubMed ID: 9429134
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.
Small KW; DeLuca AP; Whitmore SS; Rosenberg T; Silva-Garcia R; Udar N; Puech B; Garcia CA; Rice TA; Fishman GA; Héon E; Folk JC; Streb LM; Haas CM; Wiley LA; Scheetz TE; Fingert JH; Mullins RF; Tucker BA; Stone EM
Ophthalmology; 2016 Jan; 123(1):9-18. PubMed ID: 26507665
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
Khurana RN; Sun X; Pearson E; Yang Z; Harmon J; Goldberg MF; Zhang K
Ophthalmology; 2009 Oct; 116(10):1976-83. PubMed ID: 19616854
[TBL] [Abstract][Full Text] [Related]
7. North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.
Small KW; Udar N; Yelchits S; Klein R; Garcia C; Gallardo G; Puech B; Puech V; Saperstein D; Lim J; Haller J; Flaxel C; Kelsell R; Hunt D; Evans K; Lennon F; Pericak-Vance M
Mol Vis; 1999 Dec; 5():38. PubMed ID: 10617775
[TBL] [Abstract][Full Text] [Related]
8. [North Carolina macular dystrophy. Hereditary macular disease with good functional prognosis].
Schworm HD; Ulbig MW; Hoops J; Rudolph G; Weber BH; Ehrt O; Boergen KP
Ophthalmologe; 1998 Jan; 95(1):13-8. PubMed ID: 9531796
[TBL] [Abstract][Full Text] [Related]
9. Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy).
Kiernan DF; Shah RJ; Hariprasad SM; Grassi MA; Small KW; Kiernan JP; Mieler WF
Ophthalmology; 2011 Jul; 118(7):1435-43. PubMed ID: 21310494
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
Cipriani V; Kalhoro A; Arno G; Silva RS; Pontikos N; Puech V; McClements ME; Hunt DM; van Heyningen V; Michaelides M; Webster AR; Moore AT; Puech B
Ophthalmic Genet; 2017 Dec; 38(6):511-519. PubMed ID: 28635424
[TBL] [Abstract][Full Text] [Related]
11. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the
Bowne SJ; Sullivan LS; Wheaton DK; Locke KG; Jones KD; Koboldt DC; Fulton RS; Wilson RK; Blanton SH; Birch DG; Daiger SP
Mol Vis; 2016; 22():1239-1247. PubMed ID: 27777503
[TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family.
Pauleikhoff D; Sauer CG; Müller CR; Radermacher M; Merz A; Weber BH
Am J Ophthalmol; 1997 Sep; 124(3):412-5. PubMed ID: 9439376
[TBL] [Abstract][Full Text] [Related]
13. Genetic linkage studies of a North Carolina macular dystrophy family.
Audere M; Rutka K; Inaskina I; Peculis R; Sepetiene S; Valeina S; Lāce B
Medicina (Kaunas); 2016; 52(3):180-6. PubMed ID: 27496188
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy.
Rosenberg T; Roos B; Johnsen T; Bech N; Scheetz TE; Larsen M; Stone EM; Fingert JH
Mol Vis; 2010 Dec; 16():2659-68. PubMed ID: 21179233
[TBL] [Abstract][Full Text] [Related]
15. North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus.
Small KW; Puech B; Mullen L; Yelchits S
Mol Vis; 1997 Jan; 3():1. PubMed ID: 9238090
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
Griesinger IB; Sieving PA; Ayyagari R
Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):248-55. PubMed ID: 10634627
[TBL] [Abstract][Full Text] [Related]
17. North Carolina macular dystrophy is assigned to chromosome 6.
Small KW; Weber JL; Roses A; Lennon F; Vance JM; Pericak-Vance MA
Genomics; 1992 Jul; 13(3):681-5. PubMed ID: 1639395
[TBL] [Abstract][Full Text] [Related]
18. Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q.
Reichel MB; Kelsell RE; Fan J; Gregory CY; Evans K; Moore AT; Hunt DM; Fitzke FW; Bird AC
Br J Ophthalmol; 1998 Oct; 82(10):1162-8. PubMed ID: 9924305
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]