Recombinant chromosome 4 in two fetuses - case report and literature review-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Recombinant chromosome 4 in two fetuses - case report and literature review

Published:2018-08-22 Issue:1 Volume:11 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Wu Yi,Wang Yanlin,Wen Shi Wu,Zhao Xinrong,Hu Wenjing,Liu Chunmin,Gao Li,Zhang Yan,Wang Shan,Yang Xingyu,He Biwei,Cheng Weiwei

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-018-0393-1.pdf

Reference27 articles.

1. Ho KS, South ST, Lortz A, et al. Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirchhorn syndrome. J Med Genet. 2016;53:256-63.

2. Vona B, Nanda I, Neuner C, et al. Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features : review of literature. BMC Med Genet. 2014;15:1–7.

3. Beaujard MP, Jouannic JM, Bessières B, et al. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the wolf–Hirschhorn syndrome phenotype. Prenat Diagn. 2005;25:451–5.

4. Cernakova I, Kvasnicova M, Lovasova Z, et al. A duplication dup (4) (q28q35.2) de novo in a newborn. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2006;150:113–6.

5. Battaglia A, Brothman AR, Carey JC. Recombinant 4 Syndrome Due to an Unbalanced Pericentric Inversion of Chromosome 4. Am J Med Genet. 2002;106:103–6.

Cited by 3 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. Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations;Taiwanese Journal of Obstetrics and Gynecology;2024-03

2. Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication;Genes;2021-10-16

3. Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array;Molecular Cytogenetics;2020-04-10

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