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Home Search Quick Search Advanced Fulltext Browse Collections Persons My eDoc Session History Login Name: Password: Documentation Help Support Wiki Direct access to document ID:	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 The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.