Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract

Fetal and neonatal interventions (e.g., amnioinfusions, amniotic shunting, and infant dialysis) have increased survival of infants with severe Congenital Anomalies of the Kidney and Urinary Tract (CAKUT), however, outcomes vary dramatically. Our aim was to perform Whole Exome Sequencing (WES) in a u...

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Detalles Bibliográficos
Autores principales: Harris, Meredith, Schuh, Meredith P., McKinney, David, Kaufman, Kenneth, Erkan, Elif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386178/
https://www.ncbi.nlm.nih.gov/pubmed/35990004
http://dx.doi.org/10.3389/fped.2022.898773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386178/
https://www.ncbi.nlm.nih.gov/pubmed/35990004
http://dx.doi.org/10.3389/fped.2022.898773

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