Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.
Publication
, Journal Article
Hall, G; Routh, JC; Gbadegesin, RA
Published in: Am J Kidney Dis
July 2017
Duke Scholars
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Published In
Am J Kidney Dis
DOI
EISSN
1523-6838
Publication Date
July 2017
Volume
70
Issue
1
Start / End Page
8 / 10
Location
United States
Related Subject Headings
- Urology & Nephrology
- Phenotype
- Marfan Syndrome
- Humans
- DiGeorge Syndrome
- DNA Copy Number Variations
- Arachnodactyly
- 3202 Clinical sciences
- 1117 Public Health and Health Services
- 1103 Clinical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Hall, G., Routh, J. C., & Gbadegesin, R. A. (2017). Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype. Am J Kidney Dis, 70(1), 8–10. https://doi.org/10.1053/j.ajkd.2017.03.017
Hall, Gentzon, Jonathan C. Routh, and Rasheed A. Gbadegesin. “Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.” Am J Kidney Dis 70, no. 1 (July 2017): 8–10. https://doi.org/10.1053/j.ajkd.2017.03.017.
Hall G, Routh JC, Gbadegesin RA. Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype. Am J Kidney Dis. 2017 Jul;70(1):8–10.
Hall, Gentzon, et al. “Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.” Am J Kidney Dis, vol. 70, no. 1, July 2017, pp. 8–10. Pubmed, doi:10.1053/j.ajkd.2017.03.017.
Hall G, Routh JC, Gbadegesin RA. Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype. Am J Kidney Dis. 2017 Jul;70(1):8–10.
Published In
Am J Kidney Dis
DOI
EISSN
1523-6838
Publication Date
July 2017
Volume
70
Issue
1
Start / End Page
8 / 10
Location
United States
Related Subject Headings
- Urology & Nephrology
- Phenotype
- Marfan Syndrome
- Humans
- DiGeorge Syndrome
- DNA Copy Number Variations
- Arachnodactyly
- 3202 Clinical sciences
- 1117 Public Health and Health Services
- 1103 Clinical Sciences