Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis

BACKGROUND: Craniosynostosis is one of the major genetic disorders affecting 1 in 2,100–2,500 live newborn children. Environmental and genetic factors are involved in the manifestation of this disease. The suggested genetic causes of craniosynostosis are pathogenic variants in FGFR1, FGFR2, FGFR3, a...

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Detalles Bibliográficos
Publicado en:Mol Genet Genomic Med
Main Authors: Ibarra‐Arce, Aurora, Almaraz‐Salinas, Manuel, Martínez‐Rosas, Víctor, Ortiz de Zárate‐Alarcón, Gabriela, Flores‐Peña, Laura, Romero‐Valdovinos, Mirza, Olivo‐Díaz, Angélica
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2020
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Original Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7434736/
https://ncbi.nlm.nih.gov/pubmed/32510873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1266
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