Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation

Published:2007-09-12 Issue:12 Volume:27 Page:1112-1117
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Simovich Marcia J.,Yatsenko Svetlana A.,Kang Sung-Hae L.,Cheung Sau Wai,Dudek Martha E.,Pursley Amber,Ward Patricia A.,Patel Ankita,Lupski James R.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.1841/fullpdf

Reference32 articles.

1. Detection of deletions in de novo balanced chromosomes rearrangements: further evidence for their role in phenotypic abnormalities;Astbury;Genet Med,2004

2. A report of a child with a deletion 9(q34.3): a recognizable phenotype?;Ayyash;J Med Genet,1997

3. Elevated first-trimester nuchal translucency increases the risk of congenital heart defects;Bahado-Singh;Am J Obstet Gynecol,2005

4. Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization;Ballif;Prenat Diagn,2006

5. Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro;Benkhalifa;Prenat Diagn,2005

Cited by 26 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. Prenatal diagnosis via Single Nucleotide Polymorphism array analysis for fetuses from balanced translocation carriers at the second trimester;2023-11-29

2. Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells;Journal of Nanobiotechnology;2022-12-30

3. Prenatal Diagnosis of Chromosomal Abnormalities: From Karyotype to Microarray;Genetic Disorders and the Fetus;2021-04-20

4. MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV;Biomedical Papers;2021-03-31

5. Chromosomal Microarray in the New High-Throughput Technological and Bioinformatic Era;Essentials of Bioinformatics, Volume II;2019

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