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          Institute: MPI für molekulare Genetik     Collection: Research Group Development and Disease     Display Documents



  history
ID: 307740.0, MPI für molekulare Genetik / Research Group Development and Disease
A complex phenotype with cystic renal disease
Authors:Müller, D.; Klopocki, E.; Neumann, L. E.; Mundlos, Stefan; Taupitz, M.; Schulze, I.; Ropers, Hans-Hilger; Querfeld, U.; Ullmann, Reinhard
Language:English
Date of Publication (YYYY-MM-DD):2006-11-01
Title of Journal:Kidney International : Official Journal of the International Society of Nephrology
Journal Abbrev.:Kidney Int.
Volume:70
Issue / Number:9
Start Page:1656
End Page:1660
Copyright:© 2006 International Society of Nephrology
Review Status:not specified
Audience:Experts Only
Comment of the Author/Creator:Correspondence: D Müller, Department of Pediatric Nephrology, Charité Campus Virchow, Augustenburger Platz 1, Berlin 13353, Germany. E-mail: dominik.mueller@charite.de
External Publication Status:published
Document Type:Article
Communicated by:Stefan Mundlos
Affiliations:MPI für molekulare Genetik
External Affiliations:1.Department of Pediatric Nephrology, Charité Campus Virchow, Berlin, Germany;
2.Department of Medical Genetics, Charité Campus Virchow, Berlin, Germany;
3.Department of Human Genetics, Charité Campus Virchow, Berlin, Germany;
4.Department of Diagnostic and Interventional Radiology, Charité Campus Virchow, Berlin, Germany;
5.Department of Pediatric Immunology, Charité Campus Virchow, Berlin, Germany.
Identifiers:ISSN:1523-1755
DOI:10.1038/sj.ki.5001746
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