发现好书期刊，享受阅读乐趣

海量图书期刊资源，随时随地畅享阅读乐趣

A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis

Sahin, Yavuz; Güngör, Olcay; Ayaz, Akif; Güngör, Gülay; Sahin, Bedia; Yaykasli, Kursad; Ceylaner, Serdar

期刊名称Brain and Development
作者Sahin, Yavuz; Güngör, Olcay; Ayaz, Akif; Güngör, Gülay; Sahin, Bedia; Yaykasli, Kursad; Ceylaner, Serdar
印刷ISSN0387-7604
文件大小665.54KB
发表时间2016-9
DOI10.1016/j.braindev.2016.09.002