Atypical microdeletion in 22q11 deletion syndrome reveals new candidate causative genes
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference23 articles.
1. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003
2. Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements;Emanuel;Dev Disabil Res Rev,2008
3. Phenotype of adults with the 22q11 deletion syndrome: a review;Cohen;Am J Med Genet,1999
4. Role of TBX1 in human del22q11.2 syndrome;Yagi;Lancet,2003
5. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome;Gao;Hum Mol Genet,2015
Cited by 7 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. Lateral thinking in syndromic congenital cardiovascular disease;Disease Models & Mechanisms;2023-05-01
2. FaNDOM: Fast nested distance-based seeding of optical maps;Patterns;2021-05
3. FaNDOM: Fast Nested Distance-Based Seeding of Optical Maps;SSRN Electronic Journal;2021
4. A Role for SERCA Pumps in the Neurobiology of Neuropsychiatric and Neurodegenerative Disorders;Advances in Experimental Medicine and Biology;2019-10-24
5. A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome;Clinical Diabetes and Endocrinology;2019-08-13
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