Detection of MSX1 gene mutations in patients with congenital tooth loss in Van der Woude syndrome

Detection of MSX1 gene mutations in patients with congenital tooth loss in Van der Woude syndrome

Objective To explore the relationship between MSX1 gene detection and tooth loss in a Van der Woude syndrome (VWS) family. Methods DNA was extracted from the venous blood of 2 patients with dental hy⁃ podontia in the 9th family of Van der Woude syndrome (VWS) families and 62 controls with complete...

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Bibliographic Details
Main Authors: DU Xinya, LI Xiaoyu, XIE Chun, WU Bin, SONG Guangbao, DU Ye
Format: Article
Language:zho
Published: Editorial Department of Journal of Prevention and Treatment for Stomatological Diseases 2020-01-01
Series:口腔疾病防治
Subjects:
van der woude syndrome，
congenital missing teeth，
lower lip fistula，
cleft lip，
cleft palate，
msx1，
pathogenic gene，
gene polymorphism，
genetic mutations，
Online Access:http://www.kqjbfz.com/CN/10.12016/j.issn.2096-1456.2020.01.008

Internet

http://www.kqjbfz.com/CN/10.12016/j.issn.2096-1456.2020.01.008

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