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Oligonephronia and Wolf‐Hirschhorn syndrome: A further observation

  • Published:2017-11-28 Issue:2 Volume:176 Page:409-414
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am J Med Genet

Author:

Gatto Antonio1ORCID,Ferrara Pietro1,Leoni Chiara2,Onesimo Roberta2,Zollino Marcella3,Emma Francesco4,Zampino Giuseppe2

Affiliation:

1. Institute of PediatricsFondazione Policlinico Universitario A. GemelliCatholic UniversityRomeItaly

2. Center for Rare Disease and Congenital DefectsFondazione Policlinico Universitario A. GemelliCatholic UniversityRomeItaly

3. Institute of Genomic MedicineFondazione Policlinico Universitario A. GemelliCatholic UniversityRomeItaly

4. Division of Nephrology and DialysisChildren's Hospital Bambino Gesù, IRCCSRomeItaly

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Oligomeganephronia: An unexpected cause of chronic renal failure;Abdelraheem M.;Saudi Journal of Kidney Diseases and Transplantation,2004

2. Acrorenal syndrome associated with visual defect

3. A case of late-onset oligomeganephronia

4. Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome
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