Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome

Author:

Van Batavia Jason P.1ORCID,Crowley Terrence B.2ORCID,Burrows Evanette2,Zackai Elaine H.2,Sanna‐Cherchi Simone3,McDonald‐McGinn Donna M.2,Kolon Thomas F.1

Affiliation:

1. Division of UrologyChildren's Hospital of Philadelphia Philadelphia Pennsylvania

2. Division of Human GeneticsChildren's Hospital of Philadelphia Philadelphia Pennsylvania

3. Division of NephrologyNew York‐Presbyterian Hospital Columbia University Medical Center New York New York

Funder

National Center for Advancing Translational Sciences

Urology Care Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Epidemiology of hypospadias in Europe: a registry-based study

2. Update on Multicystic Dysplastic Kidney

3. The spectrum of the DiGeorge syndrome

4. Renal and urological tract malformations caused by a 22q11 deletion.

5. A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11;Driscoll D. A.;American Journal of Human Genetics,1992

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