Fetal microtia and FGFR2 polymorphism

Association of the single-nucleotide polymorphism (SNP) of rs3135718 site in fibroblast growth factor receptor 2 (FGFR2) gene with congenital microtia was investigated. A total of 193 patients with congenital microtia (observation group) and 150 normal and healthy fetuses (control group) treated in...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ruilian, Du, Peixia, Sun, Hongmei, Yang, Li, Lin, Pingzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566112/
https://www.ncbi.nlm.nih.gov/pubmed/31258676
http://dx.doi.org/10.3892/etm.2019.7568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566112/
https://www.ncbi.nlm.nih.gov/pubmed/31258676
http://dx.doi.org/10.3892/etm.2019.7568

Ejemplares similares