Copy number variations associated with fetal congenital kidney malformations

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 (SNP) a...

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Detalles Bibliográficos
Autores principales: Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Chen, Xuemei, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092440/
https://www.ncbi.nlm.nih.gov/pubmed/32211073
http://dx.doi.org/10.1186/s13039-020-00481-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092440/
https://www.ncbi.nlm.nih.gov/pubmed/32211073
http://dx.doi.org/10.1186/s13039-020-00481-7

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