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...

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Bibliographic Details
Main Authors: Tanasubsinn N., Sittiwangkul R., Pongprot Y., Kawasaki K., Ohazama A., Sastraruji T., Kaewgahya M., Kantaputra P.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029319737&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40231
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Institution: Chiang Mai University

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