A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. by Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Cristina Villanueva-Mendoza, Vianney Cortés-González, Muhammad Imran Khan, Anneke I den Hollander

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Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome by Valeria Lo Faro, Sorath N. Siddiqui, Muhammad I. Khan, Cristina Villanueva‐Mendoza, Vianney Cortés‐González, Nomdo Jansonius, Arthur A. B. Bergen, Shazia Micheal

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P418: The diagnostic journey of Mexican patients with Verheij syndrome by Karla Cifuentes-Uribe, Alejandra Reyes-De La Rosa, Rodrigo Moreno-Salgado, America Villasenor-Dominguez, Magdalena Ceron-Rodriguez, Romina Viveros-Rodriguez, Vianney Cortes-Gonzalez, Gilda Garza-Mayén

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Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants by Vasileios Toulis, Vianney Cortés-González, Marta de Castro-Miró, Juliana Ferraz Sallum, Jaume Català-Mora, Cristina Villanueva-Mendoza, Marcela Ciccioli, Roser Gonzàlez-Duarte, Rebeca Valero, Gemma Marfany

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The Genetic Landscape of Inherited Retinal Diseases in a Mexican Cohort: Genes, Mutations and Phenotypes by Cristina Villanueva-Mendoza, Miquel Tuson, David Apam-Garduño, Marta de Castro-Miró, Raul Tonda, Jean Remi Trotta, Gemma Marfany, Rebeca Valero, Vianney Cortés-González, Roser Gonzàlez-Duarte

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