SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia
Author:
Affiliation:
1. VictorianClinicalGenetics Service and Murdoch Children Institute; Melbourne Australia
2. Newborn Intensive Care Unit; Royal Children's Hospital; Melbourne Australia
3. University of Melbourne Department of Paediatrics; Melbourne Australia
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37177/fullpdf
Reference53 articles.
1. 2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic hernia;Bermudez-Wagner;Clin Dysmorph,2013
2. Associated malformations and chromosomal defects in congenital diaphragmatic hernia;Bollmann;Fetal Diagn Ther,1995
3. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature;Chen;Prenat Diagn,2004a
4. Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin;Chen;Prenat Diagn,2004b
5. PTCH1 duplication in a family with microcephaly and mild developmental delay;Derwinska;Eur J Hum Genet,2009
Cited by 19 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. Konjenital Anomali ve/veya Nörogelişimsel Geriliği olan Çocukluk Çağındaki Türk Hastalarda Kromozomal Mikroarray Deneyimi: ASXL2 Gen Duplikasyonu ve Xq13 Delesyonunun İncelenmesi;Dicle Tıp Dergisi;2024-03-14
2. Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia;Prenatal Diagnosis;2022-11-26
3. Multiple Intestinal Anomalies in a Newborn with 22q11.2 Microdeletion Syndrome: A Case Report and Literature Review;Journal of Pediatric Genetics;2022-08-02
4. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07
5. Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic Hernia;European Journal of Pediatric Surgery;2021-12
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