Prenatal diagnosis of trisomy 1q21-qter: Case report and review of literature
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference19 articles.
1. De novo interstitial direct duplication 1(q23.1q31.1) in a fetus with Pierre Robin sequence and camptodactyly
2. Duplication Dup(1)(q32q44) Detected by Comparative Genomic Hybridization (CGH): Further Delineation of Trisomies 1q
3. Confirmation of proximal 1q duplication using fluorescence in situ hybridization
4. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2
5. Congenital Ocular Defects Associated With an Abnormality of the Human Chromosome 1: Trisomy 1q32-qter
Cited by 20 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. Genomic Characterization of a Rare, de Novo Unbalanced ins(3;1)(p25.3;q21.3q23.3) in a Female Child with Multiple Congenital Anomalies;Cytogenetic and Genome Research;2020
2. De NovoTrisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies;Case Reports in Genetics;2016
3. Molecular Cytogenetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2015-11-23
4. Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangements;American Journal of Medical Genetics Part A;2014-11-26
5. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature;Birth Defects Research Part A: Clinical and Molecular Teratology;2014-02-12
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