Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?
Author:
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/s13039-019-0443-3.pdf
Reference38 articles.
1. Rasmussen M, Olsen MS, Sunde L, Sperling LS. Danish fetal medicine research G, Petersen OB. Kidney anomalies diagnosed by prenatal ultrasound screening and associated non-urinary malformations: a nationwide prevalence study. Prenat Diagn. 2016;36:847–53.
2. Nef S, Neuhaus TJ, Sparta G, Weitz M, Buder K, Wisser J, et al. Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract. Eur J Pediatr. 2016;175:667–76.
3. Verbitsky M, Kogon AJ, Matheson M, Hooper SR, Wong CS, Warady BA, et al. Genomic disorders and neurocognitive impairment in pediatric CKD. J Am Soc Nephrol. 2017;28:2303–9.
4. Verbitsky M, Sanna-Cherchi S, Fasel DA, Levy B, Kiryluk K, Wuttke M, et al. Genomic imbalances in pediatric patients with chronic kidney disease. J Clin Invest. 2015;125:2171–8.
5. de Bruyn R, Marks SD. Postnatal investigation of fetal renal disease. Semin Fetal Neonatal Med. 2008;13:133–41.
Cited by 10 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 Genetic Analysis of Fetal 17q12 Microdeletion Syndrome and Relation to Kidney Abnormalities;2023-05-25
2. Identification of complex and cryptic chromosomal rearrangements by optical genome mapping;Molecular Cytogenetics;2023-04-26
3. Prenatal Genetic Analysis of Kidney Abnormalities;2023-02-24
4. Treatment for complete bilateral duplex kidneys with severe hydronephrosis and ureterectasis of the upper moiety in a child: A case report and literature review;Frontiers in Surgery;2022-11-02
5. Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-09
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