A novel PTCH1 mutation underlies nonsyndromic cleft lip and/or palate in a Han Chinese family-Reference-Cited by-同舟云学术

A novel PTCH1 mutation underlies nonsyndromic cleft lip and/or palate in a Han Chinese family

Published:2018-07-09 Issue:7 Volume:24 Page:1318-1325
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Dis

Author:

Zhao Huaxiang¹,Zhong Wenjie¹,Leng Chuntao²,Zhang Jieni¹,Zhang Mengqi¹,Huang Wenbin¹,Zhang Yunfan¹,Li Weiran¹,Jia Peizeng¹,Lin Jiuxiang¹,Maimaitili Gulibaha²,Chen Feng³^ORCID

Affiliation:

1. Department of Orthodontics; Peking University School and Hospital of Stomatology; Beijing China

2. Department of Stomatology; The Fifth Affiliated Hospital of Xinjiang Medical University; Urumqi China

3. Central Laboratory; Peking University School and Hospital of Stomatology; Beijing China

Funder

Interdisciplinary Medicine Seed Fund of Peking University

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/odi.12915/fullpdf

Reference40 articles.

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3. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24;Birnbaum;Nature Genetics,2009

4. Mutation screening in the IRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritance;Birnbaum;American Journal of Medical Genetics Part A,2008

5. The mechanisms of Hedgehog signalling and its roles in development and disease;Briscoe;Nature Reviews Molecular Cell Biology,2013

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