Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays

BACKGROUND: While congenital anomalies of the kidney and urinary tract (CAKUT) constitute one‐third of all congenital malformations, the mechanisms underlying their development are poorly understood. Some studies have reported an association between CAKUT and copy number variations (CNVs) in childre...

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Detalles Bibliográficos
Autores principales: Cai, Meiying, Lin, Na, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, Chen, Xuemei, Dai, Yifang, Lin, Yuan, Huang, Hailong, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977156/
https://www.ncbi.nlm.nih.gov/pubmed/31506986
http://dx.doi.org/10.1002/jcla.23025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977156/
https://www.ncbi.nlm.nih.gov/pubmed/31506986
http://dx.doi.org/10.1002/jcla.23025

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