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2. Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locus. Ferrell RE; Hittner HM; Antoszyk JH Am J Hum Genet; 1983 Jan; 35(1):78-84. PubMed ID: 6823974 [TBL] [Abstract][Full Text] [Related]
3. Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family. Hou YC; Richards JE; Bingham EL; Pawar H; Scott K; Segal M; Lunetta KL; Boehnke M; Sieving PA Hum Hered; 1996; 46(4):211-20. PubMed ID: 8807324 [TBL] [Abstract][Full Text] [Related]
7. Novel Presenting Phenotype in a Child With Autosomal Dominant Best's Vitelliform Macular Dystrophy. Abdalla YF; De Salvo G; Elsahn A; Self JE Ophthalmic Surg Lasers Imaging Retina; 2017 Jul; 48(7):580-585. PubMed ID: 28728185 [TBL] [Abstract][Full Text] [Related]
8. Molecular evidence for non-penetrance in Best's disease. Weber BH; Walker D; Müller B J Med Genet; 1994 May; 31(5):388-92. PubMed ID: 8064817 [TBL] [Abstract][Full Text] [Related]
9. A recombination event excludes the ROM1 locus from the Best's vitelliform macular dystrophy region. Stöhr H; Weber BH Hum Genet; 1995 Feb; 95(2):219-22. PubMed ID: 7860071 [TBL] [Abstract][Full Text] [Related]
10. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease). Marquardt A; Stöhr H; Passmore LA; Krämer F; Rivera A; Weber BH Hum Mol Genet; 1998 Sep; 7(9):1517-25. PubMed ID: 9700209 [TBL] [Abstract][Full Text] [Related]
11. Still no evidence for heterogeneity in Best's vitelliform macular dystrophy. Graff C; Wadelius C J Med Genet; 1996 Jul; 33(7):630. PubMed ID: 8818958 [No Abstract] [Full Text] [Related]
12. The gene for Best's macular dystrophy is located at 11q13 in a Swedish family. Forsman K; Graff C; Nordström S; Johansson K; Westermark E; Lundgren E; Gustavson KH; Wadelius C; Holmgren G Clin Genet; 1992 Sep; 42(3):156-9. PubMed ID: 1395087 [TBL] [Abstract][Full Text] [Related]
13. Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci. Graff C; Forsman K; Larsson C; Nordström S; Lind L; Johansson K; Sandgren O; Weissenbach J; Holmgren G; Gustavson KH Genomics; 1994 Dec; 24(3):425-34. PubMed ID: 7713492 [TBL] [Abstract][Full Text] [Related]
15. Best's vitelliform dystrophy (VMD2) maps between D11S903 and PYGM: no evidence for locus heterogeneity. Weber BH; Walker D; Müller B; Mar L Genomics; 1994 Mar; 20(2):267-74. PubMed ID: 8020974 [TBL] [Abstract][Full Text] [Related]
16. Various fundus manifestations in a Japanese family with Best's vitelliform macular dystrophy. Shibuya Y; Hayasaka S Jpn J Ophthalmol; 1993; 37(4):478-84. PubMed ID: 8145393 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene. Eksandh L; Bakall B; Bauer B; Wadelius C; Andréasson S Ophthalmic Genet; 2001 Jun; 22(2):107-15. PubMed ID: 11449320 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]