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

Abstract 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,...

Full description

Bibliographic Details
Main Authors: Aurora Ibarra‐Arce, Manuel Almaraz‐Salinas, Víctor Martínez‐Rosas, Gabriela Ortiz de Zárate‐Alarcón, Laura Flores‐Peña, Mirza Romero‐Valdovinos, Angélica Olivo‐Díaz
Format: Article
Published: Wiley 2020-08-01
Series:Molecular Genetics & Genomic Medicine
Online Access: