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8. Hypotrichosis with Juvenile Macular Dystrophy in a Patient with Cadherin 3 (CDH3) Mutation. Rishi E; Goel S; Bassi S; Rishi P Nepal J Ophthalmol; 2022 Jan; 14(27):168-172. PubMed ID: 35996915 [TBL] [Abstract][Full Text] [Related]
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10. Hypotrichosis with juvenile macular dystrophy: clinical and electrophysiological assessment of visual function. Leibu R; Jermans A; Hatim G; Miller B; Sprecher E; Perlman I Ophthalmology; 2006 May; 113(5):841-7.e3. PubMed ID: 16650681 [TBL] [Abstract][Full Text] [Related]
12. Multimodal Approach to Monitoring and Investigating Cone Structure and Function in an Inherited Macular Dystrophy. Ziccardi L; Giannini D; Lombardo G; Serrao S; Dell'Omo R; Nicoletti A; Bertelli M; Lombardo M Am J Ophthalmol; 2015 Aug; 160(2):301-312.e6. PubMed ID: 25908487 [TBL] [Abstract][Full Text] [Related]
13. A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophy. Indelman M; Bergman R; Lurie R; Richard G; Miller B; Petronius D; Ciubutaro D; Leibu R; Sprecher E J Invest Dermatol; 2002 Nov; 119(5):1210-3. PubMed ID: 12445216 [TBL] [Abstract][Full Text] [Related]
14. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report. Blanco-Kelly F; Rodrigues-Jacy da Silva L; Sanchez-Navarro I; Riveiro-Alvarez R; Lopez-Martinez MA; Corton M; Ayuso C BMC Med Genet; 2017 Jan; 18(1):1. PubMed ID: 28061825 [TBL] [Abstract][Full Text] [Related]
15. Multimodal imaging and multifocal electroretinography demonstrate autosomal recessive Stargardt disease may present like occult macular dystrophy. Sisk RA; Leng T Retina; 2014 Aug; 34(8):1567-75. PubMed ID: 24743636 [TBL] [Abstract][Full Text] [Related]
16. Hypotrichosis with juvenile macular dystrophy: Combination of whole-genome sequencing and genome-wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole-exome sequencing-A lesson from next-generation sequencing. Saeidian AH; Vahidnezhad H; Youssefian L; Sotudeh S; Sargazi M; Zeinali S; Uitto J Mol Genet Genomic Med; 2019 Nov; 7(11):e975. PubMed ID: 31560841 [TBL] [Abstract][Full Text] [Related]
17. Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome. Scheidecker S; Hull S; Perdomo Y; Studer F; Pelletier V; Muller J; Stoetzel C; Schaefer E; Defoort-Dhellemmes S; Drumare I; Holder GE; Hamel CP; Webster AR; Moore AT; Puech B; Dollfus HJ Am J Ophthalmol; 2015 Aug; 160(2):364-372.e1. PubMed ID: 25982971 [TBL] [Abstract][Full Text] [Related]
18. Cone abnormalities in fundus albipunctatus associated with RDH5 mutations assessed using adaptive optics scanning laser ophthalmoscopy. Makiyama Y; Ooto S; Hangai M; Ogino K; Gotoh N; Oishi A; Yoshimura N Am J Ophthalmol; 2014 Mar; 157(3):558-70.e1-4. PubMed ID: 24246574 [TBL] [Abstract][Full Text] [Related]
19. Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram". Vincent A; Wright T; Garcia-Sanchez Y; Kisilak M; Campbell M; Westall C; Héon E Invest Ophthalmol Vis Sci; 2013 Jan; 54(1):898-908. PubMed ID: 23221069 [TBL] [Abstract][Full Text] [Related]
20. Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy. Halford S; Holt R; Németh AH; Downes SM Arch Ophthalmol; 2012 Nov; 130(11):1490-2. PubMed ID: 23143461 [No Abstract] [Full Text] [Related] [Next] [New Search]