Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1→q24 in different offspring
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference11 articles.
1. Congenital Blepharophimosis Associated with a Unique Generalized Myopathy
2. Schwartz syndrome: Myotonia with blepharophimosis and limitation of joints
3. High Resolution of Human Chromosomes
4. Quantitative analysis of high-resolution trypsin-Giemsa bands on human prometaphase chromosomes
5. Report of the committee on the genetic constitution of chromosomes 7, 8, and 9
Cited by 42 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. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion;Gene;2014-02
2. Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions;Orphanet Journal of Rare Diseases;2013-05-16
3. A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies;American Journal of Medical Genetics Part A;2013-01-15
4. Microdeletion 3q Syndrome;Journal of Craniofacial Surgery;2011-11
5. Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions;American Journal of Medical Genetics Part A;2010-12-15
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