Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Eur Urol Open Sci
; 44: 106-112, 2022 Oct.
Article
em En
| MEDLINE
| ID: mdl-36185583
BAF, B allele frequency; CAKUT, Congenital anomalies of the kidneys and urinary tract; CNV, Copy number variations; Congenital anomalies of the kidney and urinary tract; Copy number variation; GD-CNV, Genomic disorders copy number variation; IRB, Institutional review board; Monogenic disease causation; Renal developmental; Vesicoureteral reflux; WES, Whole-exome sequencing; Whole-exome sequencing
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Tipo de estudo:
Diagnostic_studies
/
Prognostic_studies
Idioma:
En
Revista:
Eur Urol Open Sci
Ano de publicação:
2022
Tipo de documento:
Article