Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion

Published:2010-06-28 Issue:10 Volume:25 Page:3430-3433
ISSN:1460-2385
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Loirat Chantal,Bellanné-Chantelot Christine,Husson Isabelle,Deschênes Georges,Guigonis Vincent,Chabane Nadia

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/25/10/3430/17107722/gfq380.pdf

Reference32 articles.

1. Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations;Bellanné-Chantelot;Ann Intern Med,2004

2. Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5;Bellanné-Chantelot;Diabetes,2005

3. Mutations in hepatocyte nuclear factor-1beta and their related phenotypes;Edghill;J Med Genet,2006

4. Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort;Ulinski;J Am Soc Nephrol,2006

5. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys;Decramer;J Am Soc Nephrol,2007

Cited by 73 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 perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion;Taiwanese Journal of Obstetrics and Gynecology;2024-01

2. Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominant Polycystic Kidney Disease;Canadian Journal of Kidney Health and Disease;2024-01

3. Review of neurodevelopmental disorders in patients with HNF1B gene variations;Frontiers in Pediatrics;2023-03-09

4. The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored;Cells;2023-01-13

5. A Case of Diabetes Mellitus Type MODY5 as a feature of 17q12 Deletion Syndrome;Journal of Clinical Research in Pediatric Endocrinology;2022-12-13

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