Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene

Published:2019-03 Issue:2 Volume:58 Page:292-295
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Sun Manna,Lou Jiwu,Li Qiaoyi,Chen Jianhong,Li Yujuan,Li Dongzhi,Yuan Haiming,Liu Yanhui

Funder

Social Developmental Project of Donguan

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference18 articles.

1. Paper 4: EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe;Loane;Birth Defects Res A Clin Mol Teratol,2011

2. Outcome following prenatal diagnosis of severe bilateral renal hypoplasia;Spaggiari;Prenat Diagn,2013

3. Epidemiology of chronic renal failure in children: data from the ItalKid project;Ardissino;Pediatrics,2003

4. Copy-number disorders are a common cause of congenital kidney malformations;Sanna-Cherchi;Am J Hum Genet,2012

5. Developmental genetics and congenital anomalies of the kidney and urinary tract;Uy;J Pediatr Genet,2016

Cited by 8 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. Genome-Wide Association Study of the Risk of Schizophrenia in the Republic of Bashkortostan;Russian Journal of Genetics;2023-08

2. Genome-Wide Association Study of the Risk of Schizophrenia in the Republic of Bashkortostan;Генетика;2023-08-01

3. Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene;Molecular Cytogenetics;2022-12-21

4. Novel somatic PBX1 mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasia;Clinical Kidney Journal;2022-04-06

5. De novo PBX1 variant in a patient with glaucoma, kidney anomalies, and developmental delay: An expansion of the CAKUTHED phenotype;American Journal of Medical Genetics Part A;2021-11-19

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