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Year Number of Results
2016 2
2018 2
2019 4
2020 3
2021 2
2022 2
2024 0

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14 results

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Page 1
Bilateral Vision Loss in a Young Patient.
Cárdenas-Belaunzarán J, Turcio-Aceves O, Cortés-González V. Cárdenas-Belaunzarán J, et al. Among authors: cortes gonzalez v. J Neuroophthalmol. 2022 Jun 1;42(2):e527. doi: 10.1097/WNO.0000000000001579. Epub 2022 Mar 22. J Neuroophthalmol. 2022. PMID: 35421026 No abstract available.
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
Bahena P, Daftarian N, Maroofian R, Linares P, Villalobos D, Mirrahimi M, Rad A, Doll J, Hofrichter MAH, Koparir A, Röder T, Han S, Sabbaghi H, Ahmadieh H, Behboudi H, Villanueva-Mendoza C, Cortés-Gonzalez V, Zamora-Ortiz R, Kohl S, Kuehlewein L, Darvish H, Alehabib E, Arenas-Sordo ML, Suri F, Vona B, Haaf T. Bahena P, et al. Among authors: cortes gonzalez v. Hum Genet. 2022 Apr;141(3-4):785-803. doi: 10.1007/s00439-021-02303-1. Epub 2021 Jun 20. Hum Genet. 2022. PMID: 34148116 Free PMC article.
The relevance of the cytogenetic analysis in syndromic microphthalmia/anophthalmia.
Apam-Garduño D, Cortés-González V, Quintana-Fernández L, Martínez-Anaya D, Pérez-Vera P, Villanueva-Mendoza C. Apam-Garduño D, et al. Among authors: cortes gonzalez v. Ophthalmic Genet. 2019 Dec;40(6):584-587. doi: 10.1080/13816810.2019.1698618. Epub 2019 Dec 6. Ophthalmic Genet. 2019. PMID: 31809626 No abstract available.
Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants.
Toulis V, Cortés-González V, Castro-Miró M, Sallum JF, Català-Mora J, Villanueva-Mendoza C, Ciccioli M, Gonzàlez-Duarte R, Valero R, Marfany G. Toulis V, et al. Among authors: cortes gonzalez v. Genes (Basel). 2020 Mar 31;11(4):378. doi: 10.3390/genes11040378. Genes (Basel). 2020. PMID: 32244552 Free PMC article.
14 results