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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

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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, 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.
Journal cover image

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