Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gabriela Ortiz de Zarate-Alarcón"'
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:
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