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Méndez-Hernández CD 9

Showing records 1 to 9 | Display all abstracts from Méndez-Hernández CD

61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Medina-Trillo C
European Journal of Human Genetics 2016; 24: 672-680

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61077 Pigment dispersion syndrome associated with optic nerve melanocytoma
Asorey-García A
Archivos de la Sociedad Española de Oftalmologia 2015; 90: 484-486

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61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Aroca-Aguilar JD
European Journal of Human Genetics 2016; 24: 672-680

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61077 Pigment dispersion syndrome associated with optic nerve melanocytoma
Méndez-Hernández CD
Archivos de la Sociedad Española de Oftalmologia 2015; 90: 484-486

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61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Méndez-Hernández CD
European Journal of Human Genetics 2016; 24: 672-680

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61077 Pigment dispersion syndrome associated with optic nerve melanocytoma
Santos-Bueso E
Archivos de la Sociedad Española de Oftalmologia 2015; 90: 484-486

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61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Morales L
European Journal of Human Genetics 2016; 24: 672-680

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61077 Pigment dispersion syndrome associated with optic nerve melanocytoma
García-Feijoo J
Archivos de la Sociedad Española de Oftalmologia 2015; 90: 484-486

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61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
García-Antón M; García-Feijoo J; Escribano J
European Journal of Human Genetics 2016; 24: 672-680

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