Work

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

Year: 2017

Type: article

Source: American Journal of Kidney Diseases

DOI: 10.1053/j.ajkd.2017.03.017

Authors: Gentzon Hall, Jonathan C. Routh, Rasheed A. Gbadegesin

Institutions: Duke University, Duke Medical Center

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funder: National Institute of Diabetes and Digestive and Kidney Diseases

Awards: George M. O'Brien Kidney Research Core Centers, Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis, Comparative Effectiveness of Vesicoureteral Reflux Treatments in Children, Functional and Phenotypic Characterization of a New FSGS Gene

OpenAlex ID: W2608704577

FWCI:

Cites: 25

Cited by: 2

Related to: 10