TFAP2B mutation and dental anomalies

© 2017 The Japan Society of Human Genetics All rights reserved. Mutations inTFAP2B has been reported in patients with isolated patent ductus arteriosus (PDA) and Char syndrome. We performed mutation analysis of TFAP2B in 43 patients with isolated PDA, 7 patients with PDA with other congenital heart...

Full description

Saved in:
Bibliographic Details
Main Authors: Natchaya Tanasubsinn, Rekwan Sittiwangkul, Yupada Pongprot, Katsushige Kawasaki, Atsushi Ohazama, Thanapat Sastraruji, Massupa Kaewgahya, Piranit Nik Kantaputra
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029319737&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46365
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University