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  Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype
 
 
Title: Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype
Author: Hall, Gentzon
Routh, Jonathan C.
Gbadegesin, Rasheed A.
Appeared in: American journal of kidney diseases
Paging: Volume 70 (2017) nr. 1 pages 3 p.
Year: 2017
Contents:
Publisher: National Kidney Foundation, Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 30 of 31 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands