Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.
Published
Journal Article
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
- 28456345
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