Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24-Reference-Cited by-同舟云学术

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Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24

Published:2009-12-10 Issue:5 Volume:25 Page:1496-1501
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Ashraf S.,Hoskins B. E.,Chaib H.,Hoefele J.,Pasch A.,Saisawat P.,Trefz F.,Hacker H. W.,Nuernberg G.,Nuernberg P.,Otto E. A.,Hildebrandt F.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/25/5/1496/5203783/gfp650.pdf

Reference43 articles.

1. Malformations in newborn: results based on 30940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)

2. Renal abnormalities and their developmental origin

3. Toward an etiological classification of developmental disorders of the kidney and upper urinary tract

4. A molecular and genetic view of human renal and urinary tract malformations

Cited by 17 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. The Urinary System;Keeling's Fetal and Neonatal Pathology;2022

2. Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux;Journal of the American Society of Nephrology;2021-02-17

3. The Frequency of Familial Congenital Anomalies of the Kidney and Urinary Tract: Should We Screen Asymptomatic First-Degree Relatives Using Urinary Tract Ultrasonography?;Nephron;2020

4. Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux;Scientific Reports;2017-11-03

5. Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney;Kidney International;2015-12

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