RUNX2 mutations in Chinese patients with cleidocranial dysplasia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

RUNX2 mutations in Chinese patients with cleidocranial dysplasia

Published:2009-06-10 Issue:5 Volume:24 Page:425-431
ISSN:0267-8357
Container-title:Mutagenesis
language:en
Short-container-title:Mutagenesis

Author:

Li Y.,Pan W.,Xu W.,He N.,Chen X.,Liu H.,Darryl Quarles L.,Zhou H.,Xiao Z.

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Genetics(clinical),Toxicology,Genetics

Link

http://academic.oup.com/mutage/article-pdf/24/5/425/5548717/gep025.pdf

Reference52 articles.

1. Mutations in theRUNX2 gene in patients with cleidocranial dysplasia

2. Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature

3. Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminalRUNX2 mutations

4. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia

5. Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sequencing analysis of exons 5 and 6 in RUNX2 in non-syndromic patients with supernumerary tooth in Kelantan, Malaysia;Clinical Oral Investigations;2021-08-28

2. A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia;ARCH ORAL BIOL;2018

3. NovelRUNX2frameshift mutations in Chinese patients with cleidocranial dysplasia;European Journal of Oral Sciences;2013-04-25

4. Cleidocranial dysplasia: a review of the dental, historical, and practical implications with an overview of the South African experience;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2013-01

5. A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia;Genetics and Molecular Research;2011

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3