PAX2 mutations in oligomeganephronia-Reference-Cited by-同舟云学术

PAX2 mutations in oligomeganephronia

Published:2001-02 Issue:2 Volume:59 Page:457-462
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Salomon Rémi,Tellier Anne-Lorraine,Attie-Bitach Tania,Amiel Jeanne,Vekemans Michel,Lyonnet Stanislas,Dureau Pascal,Niaudet Patrick,Gubler Marie-Claire,Broyer Michel

Publisher

Elsevier BV

Subject

Nephrology

Reference24 articles.

1. Bilateral renal hypoplasia with oligonephronia;Royer;Arch Fr Pediatr,1967

2. Deficient metanephric blastema: A cause of oligomeganephronia?;Foster;Pediatr Pathol,1994

3. Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1;Abdelhak;Hum Mol Genet,1997

4. A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia;Miltenyi;Eur J Pediatr,1984

5. Oligomeganephronia associated with 4p deletion type chromosomal anomaly;Park;Pediatr Pathol,1993

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