Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.

Journal Article (Editorial)

Full Text

Duke Authors

Cited Authors

  • Hall, G; Routh, JC; Gbadegesin, RA

Published Date

  • July 2017

Published In

Volume / Issue

  • 70 / 1

Start / End Page

  • 8 - 10

PubMed ID

  • 28456345

Pubmed Central ID

  • PMC5890439

Electronic International Standard Serial Number (EISSN)

  • 1523-6838

Digital Object Identifier (DOI)

  • 10.1053/j.ajkd.2017.03.017

Language

  • eng

Conference Location

  • United States