受强制性开放获取政策约束的文章 - Vianney Cortés-González了解详情
可在其他位置公开访问的文章：3 篇
Increasing the genetic diagnosis yield in inherited retinal dystrophies: assigning pathogenicity to novel non-canonical splice site variants
V Toulis, V Cortés-González, M de Castro-Miró, J Ferraz Sallum, ...
Genes 11 (4), 378, 2020
强制性开放获取政策： Government of Spain
Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome
V Lo Faro, SN Siddiqui, MI Khan, C Villanueva‐Mendoza, ...
Molecular genetics & genomic medicine 8 (7), e1215, 2020
强制性开放获取政策： European Commission
Homozygosity for a hypomorphic mutation in frizzled class receptor 5 causes syndromic ocular coloboma with microcornea in humans
V Cortés-González, M Rodriguez-Morales, P Ataliotis, C Mayer, ...
Human Genetics 143 (12), 1509-1521, 2024
强制性开放获取政策： Wellcome Trust
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