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Whole-Exome Sequencing of 21 Families: Candidate Genes for Early-Onset High Myopia.
Int J Mol Sci. 2023 Oct 27;24(21):15676. doi: 10.3390/ijms242115676.
Int J Mol Sci. 2023.
PMID: 37958660
Free PMC article.
Whole-Exome Sequencing of 24 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Keratoconus.
González-Atienza C, Sánchez-Cazorla E, Villoldo-Fernández N, Del Hierro A, Boto A, Guerrero-Carretero M, Nieves-Moreno M, Arruti N, Rodríguez-Solana P, Mena R, Rodríguez-Jiménez C, Rosa-Pérez I, Acal JC, Blasco J, Naranjo-Castresana M, Ruz-Caracuel B, Montaño VEF, Ortega Patrón C, Rubio-Martín ME, García-Fernández L, Rikeros-Orozco E, Gómez-Cano MLÁ, Delgado-Mora L, Noval S, Vallespín E.
González-Atienza C, et al. Among authors: gomez cano mla.
Genes (Basel). 2023 Sep 22;14(10):1838. doi: 10.3390/genes14101838.
Genes (Basel). 2023.
PMID: 37895187
Free PMC article.
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Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts.
Rodríguez-Solana P, Arruti N, Nieves-Moreno M, Mena R, Rodríguez-Jiménez C, Guerrero-Carretero M, Acal JC, Blasco J, Peralta JM, Del Pozo Á, Montaño VEF, Dios-Blázquez L, Fernández-Alcalde C, González-Atienza C, Sánchez-Cazorla E, Gómez-Cano MLÁ, Delgado-Mora L, Noval S, Vallespín E.
Rodríguez-Solana P, et al. Among authors: gomez cano mla.
Int J Mol Sci. 2023 Jul 13;24(14):11429. doi: 10.3390/ijms241411429.
Int J Mol Sci. 2023.
PMID: 37511188
Free PMC article.
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Expanding the Phenotypic Spectrum of Alazami Syndrome: Two Unrelated Spanish Families.
Soengas-Gonda E, Pérez de la Fuente R, Arteche-López A, Gómez-Cano MLÁ, Quesada-Espinosa JF, Palma Milla C, Lezana Rosales JM, Mayo de Andrés S, Sánchez-Calvín MT, Gómez-Rodríguez MJ, Sierra Tomillo O, Juarez Rufian A, Ramos Gomez P, Herrero-Forte C, Fenollar-Cortés M, Cotarelo-Pérez C, García Ron A, Pérez Rodríguez O, Oancea-Ionescu R, Moreno-García M.
Soengas-Gonda E, et al. Among authors: gomez cano mla.
Neuropediatrics. 2023 Feb;54(1):31-36. doi: 10.1055/a-1947-8411. Epub 2022 Sep 20.
Neuropediatrics. 2023.
PMID: 36126956
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MAST1 variant causes mega-corpus-callosum syndrome with cortical malformations but without cerebellar hypoplasia.
Rodríguez-García ME, Cotrina-Vinagre FJ, Gómez-Cano MLÁ, Martínez de Aragón A, Martín-Hernández E, Martínez-Azorín F.
Rodríguez-García ME, et al. Among authors: gomez cano mla.
Am J Med Genet A. 2020 Jun;182(6):1483-1490. doi: 10.1002/ajmg.a.61560. Epub 2020 Mar 21.
Am J Med Genet A. 2020.
PMID: 32198973
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