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Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis.
Albakri A, Pisuchpen P, Capasso JE, Schneider A, Kopinsky S, Glaser T, Chiang JP, Yomai AA, McNear D, Levin AV. Albakri A, et al. Among authors: levin av. Am J Med Genet A. 2023 Apr;191(4):1007-1012. doi: 10.1002/ajmg.a.63108. Epub 2023 Jan 3. Am J Med Genet A. 2023. PMID: 36595661 Free PMC article.
Mutations in AGBL5 associated with Retinitis pigmentosa.
Paredes DI, Bello NR, Capasso JE, Procopio R, Levin AV. Paredes DI, et al. Among authors: levin av. Ophthalmic Genet. 2023 Dec 11:1-6. doi: 10.1080/13816810.2023.2291687. Online ahead of print. Ophthalmic Genet. 2023. PMID: 38078364
Genetics of the anterior segment dysgenesis.
Paredes DI, Capasso JE, Wyman CS, Levin AV. Paredes DI, et al. Among authors: levin av. Taiwan J Ophthalmol. 2023 Jul 18;13(4):500-504. doi: 10.4103/tjo.TJO-D-23-00062. eCollection 2023 Oct-Dec. Taiwan J Ophthalmol. 2023. PMID: 38249510 Free PMC article. Review.
Ophthalmologic findings in the Cornelia de Lange syndrome.
Levin AV, Seidman DJ, Nelson LB, Jackson LG. Levin AV, et al. J Pediatr Ophthalmol Strabismus. 1990 Mar-Apr;27(2):94-102. doi: 10.3928/0191-3913-19900301-11. J Pediatr Ophthalmol Strabismus. 1990. PMID: 2348318
The SBU report: a different view.
Levin AV. Levin AV. Acta Paediatr. 2017 Jul;106(7):1037-1039. doi: 10.1111/apa.13834. Epub 2017 Apr 19. Acta Paediatr. 2017. PMID: 28301061 No abstract available.
303 results