Diagnosis and treatment of <scp>MN1</scp> C‐terminal truncation syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Diagnosis and treatment of MN1 C‐terminal truncation syndrome

Published:2022-09-20 Issue:11 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Yu Jingjia¹^ORCID,Li Chen¹,Chen Jialin¹,Ran Qiuchi¹,Zhao Yingya¹,Cao Qingxin¹,Chen Ximeng¹,Yu Linnan¹,Li Wenyang²,Zhao Zhenjin¹^ORCID

Affiliation:

1. The First Clinic, Orthodontic Department School and Hospital of Stomatology, China Medical University, Liaoning Province Key Laboratory of Oral Disease Shenyang China

2. Institute of Respiratory Disease The First Hospital of China Medical University Shenyang China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1965

Reference17 articles.

1. Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving theMN1gene

2. MN1, a novel player in human AML

3. Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma;Lekanne Deprez R. H.;Oncogene,1995

Cited by 1 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. Distinctive Craniofacial and Oral Anomalies in MN1 C-terminal Truncation Syndrome;CHIN J DENT RES;2024

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