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.
Styl ChicagoHall, Gentzon, Jonathan C. Routh, a 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 2017.
Citace podle MLAHall, Gentzon, Jonathan C. Routh, a 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 2017.
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