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...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2020-03-01
coleção:	Molecular Cytogenetics
Assuntos:	Copy-number variations Etiology Chromosomal microarray analysis Renal hypodysplasia
Acesso em linha:	http://link.springer.com/article/10.1186/s13039-020-00481-7
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!