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22. 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]
23. Abnormal dark-adapted electroretinogram in Best's vitelliform macular degeneration. Lachapelle P; Quigley MG; Polomeno RC; Little JM Can J Ophthalmol; 1988 Oct; 23(6):279-84. PubMed ID: 3203242 [TBL] [Abstract][Full Text] [Related]
24. "Novel p.Tyr284Cys BEST1 genotype-phenotype correlations of Vitelliform Macular Dystrophy in a family with incomplete penetrance". Garza-Garza LA; León-Cachón RBR; Aguirre-Garza M; Garza-Leon M Ophthalmic Genet; 2020 Apr; 41(2):183-188. PubMed ID: 32207364 [No Abstract] [Full Text] [Related]
25. 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]
26. 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]
27. Clinical and molecular genetic analysis of best vitelliform macular dystrophy. Boon CJ; Theelen T; Hoefsloot EH; van Schooneveld MJ; Keunen JE; Cremers FP; Klevering BJ; Hoyng CB Retina; 2009 Jun; 29(6):835-47. PubMed ID: 19357557 [TBL] [Abstract][Full Text] [Related]
28. Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene. Ayyagari R; Griesinger IB; Bingham E; Lark KK; Moroi SE; Sieving PA Arch Ophthalmol; 2000 Jan; 118(1):85-92. PubMed ID: 10636420 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. [Adult form of Best's vitelliform macular dystrophy--case reports]. Kolár P; Vlková E Cesk Slov Oftalmol; 2004 Jul; 60(4):300-6. PubMed ID: 15369268 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. [Vitelline macular degeneration and Best's macular degeneration are the same disease (author's transl)]. Jaeger W; Bischoff E Klin Monbl Augenheilkd; 1977 Jun; 170(6):890-9. PubMed ID: 894995 [TBL] [Abstract][Full Text] [Related]
35. In vivo microscopy of Best's Vitelliform Macular Dystrophy: optical coherence tomography study of combined stage III and IV lesions. Arora R; Das S; Shroff D; Narula R; Chauhan D Clin Exp Ophthalmol; 2007 Apr; 35(3):287-8. PubMed ID: 17430522 [TBL] [Abstract][Full Text] [Related]
36. A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34. Zhang K; Bither PP; Park R; Donoso LA; Seidman JG; Seidman CE Arch Ophthalmol; 1994 Jun; 112(6):759-64. PubMed ID: 8002833 [TBL] [Abstract][Full Text] [Related]