Genitourinary Malformations in Chromosome 22q11.2 Deletion
Author:
Affiliation:
1. From the Divisions of Pediatric Urology, Radiology and Human Genetics and Molecular Biology, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Urology
Reference9 articles.
1. The Philadelphia story: the 22q11.2 deletion: report on 250 patients;McDonald-McGinn;Genet Couns,1999
2. Renal and urological tract malformations caused by a 22q11 deletion;Devriendt;J Med Genet,1996
3. Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletion;Stewart;Teratology,1999
4. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet,1997
5. Anomalies of the kidney;Koff,1996
Cited by 46 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 and outcomes in fetuses with duplex kidney;International Journal of Gynecology & Obstetrics;2024-01-08
2. An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience;Journal of Clinical Research in Pediatric Endocrinology;2023-08-23
3. Insufficiency of Mrpl40 disrupts testicular structure and semen parameters in a murine model;Asian Journal of Andrology;2023
4. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort;Ultrasound in Obstetrics & Gynecology;2022-02
5. Clinical aspects of 22q11.2 microdeletion syndrome;ORVOSI HETILAP;2022
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