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          Institute: MPI für molekulare Genetik     Collection: Department of Human Molecular Genetics     Display Documents



  history
ID: 224423.0, MPI für molekulare Genetik / Department of Human Molecular Genetics
Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation
Authors:Kleefstra, T.; Yntema, H. G.; Oudakker, A. R.; Banning, M. J. G.; Kalscheuer, Vera M.; Chelly, J.; Moraine, C.; Ropers, Hans-Hilger; Fryns, J-P; Janssen, I. M. J.; Sistermans, E. A.; Nillesen, W. N.; de Vries, L. B. A.; Hamel, B. C. J.; van Bokhoven, H.
Language:English
Date of Publication (YYYY-MM-DD):2004-01-18
Title of Journal:Journal of Medical Genetics
Journal Abbrev.:J. Med. Genet.
Volume:41
Issue / Number:5
Start Page:394
End Page:399
Copyright:© 2004 BMJ Publishing Group Ltd
Review Status:not specified
Audience:Experts Only
Free Keywords:MRX; translocation t(X; 9); XLMR; Xp11.23; ZNF81
External Publication Status:published
Document Type:Article
Communicated by:Hans-Hilger Ropers
Affiliations:MPI für molekulare Genetik
External Affiliations:Department of Human Genetics, University Medical Centre St Radboud, Nijmegen, The Netherlands;
Département de Génétique et Pathologie Moléculaire, Institut Cochin (IC), Paris, France;
Unité de Génétique, CHU Bretonneau, Tours, France;
Centre for Human Genetics, University Hospital Leuven, Leuven, Belgium.
Identifiers:ISSN:1468-6244
DOI:10.1136/jmg.2003.016972
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