Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laura Flores‐Peña"'
Autor:
Aurora Ibarra‐Arce, Manuel Almaraz‐Salinas, Víctor Martínez‐Rosas, Gabriela Ortiz de Zárate‐Alarcón, Laura Flores‐Peña, Mirza Romero‐Valdovinos, Angélica Olivo‐Díaz
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
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 cranio
Externí odkaz:
https://doaj.org/article/5201203379754ede87ee8603862f2ae3
Autor:
Angélica Olivo-Díaz, Mirza Romero-Valdovinos, Manuel Almaraz-Salinas, Laura Flores-Peña, Víctor Martínez-Rosas, Aurora Ibarra-Arce, Gabriela Ortiz de Zarate-Alarcón
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
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 craniosynostosi
Autor:
Mirza Romero-Valdovinos, Martín García-Álvarez, Daniel Cortés-González, Sandra Sánchez-Camacho, Aurora Ibarra-Arce, Angélica Olivo-Díaz, Laura Flores-Peña, Gabriela Ortiz de Zarate-Alarcón, Silvia Arenas-Díaz
Publikováno v:
Meta Gene
Cleft lip with or without cleft palate (CL/P) is one of the most common birth defects; it is a multifactorial disease affecting > 1/1,000 live births in Europe, and its etiology is largely unknown, although it is very likely genetic and environmental
Autor:
Laura Flores-Peña, Aurora Ibarra-Arce, Mirza Romero-Valdovinos, Angélica Olivo-Díaz, G. Ortiz de Zárate-Alarcón, F. Martínez-Hernández
Publikováno v:
Genetics and molecular research : GMR. 14(1)
Apert syndrome (AS) is a frequent acrocephalosyndactyly, with autosomal dominant inheritance. AS has been associated with mutations in fibroblast growth factor receptor 2 (FGFR2), and approximately 99% of cases show 2 of the frequent mutations locate