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



  history
ID: 24374.0, MPI für molekulare Genetik / Department of Human Molecular Genetics
In-frame deletion in MECP2 causes mild nonspecific mental retardation
Authors:Yntema, Helger G.; Oudakker, Astrid R.; Kleefstra, Tjitske; Hamel, Ben C. J.; van Bokhoven, Hans; Chelly, Jamel; Kalscheuer, Vera M.; Fryns, Jean-Pierre; Raynaud, Martine; Moizard, Marie-Pierre; Moraine, Claude
Language:English
Date of Publication (YYYY-MM-DD):2002-01
Title of Journal:American Journal of Medical Genetics
Volume:107
Issue / Number:1
Start Page:81
End Page:83
Review Status:not specified
Audience:Experts Only
Abstract / Description:No abstract.
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 Nijmegen, The Netherlands
INSERM 129-ICGM, Faculté de Médecine Cochin, Paris, France
Center for Human Genetics, University of Leuven, Leuven, Belgium
Service de Génétique CHU Bretonneau, Tours, France
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