Copy number variations associated with fetal congenital kidney malformations

Copy number variations associated with fetal congenital kidney malformations

Abstract Background Congenital anomalies of the kidney and urinary tract (CAKUT) constitute 20–30% of all congenital malformations. Within the CAKUT phenotypic spectrum, renal hypodysplasia (RHD) is particularly severe. This study aimed to evaluate the applicability of single-nucleotide polymorphism...

Full description

Bibliographic Details
Main Authors: Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu
Format: Article
Language:English
Published: BMC 2020-03-01
Series:Molecular Cytogenetics
Subjects:
Copy-number variations
Etiology
Chromosomal microarray analysis
Renal hypodysplasia
Online Access:http://link.springer.com/article/10.1186/s13039-020-00481-7

Internet

http://link.springer.com/article/10.1186/s13039-020-00481-7

Similar Items