HAL Id: hal-00573454
https://hal.archives-ouvertes.fr/hal-00573454
Submitted on 4 Mar 2011
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Cohen syndrome diagnosis using whole genome arrays
Nuria Rivera-Brugués, Beate Albrecht, Dagmar Wieczorek, Heinrich Schmidt, Thomas Keller, Ina Göhring, Arif B. Ekici, Andreas Tzschach, Masoud
Garshasbi, Kathlen Franke, et al.
To cite this version:
Nuria Rivera-Brugués, Beate Albrecht, Dagmar Wieczorek, Heinrich Schmidt, Thomas Keller, et al..
Cohen syndrome diagnosis using whole genome arrays. Journal of Medical Genetics, BMJ Publishing
Group, 2010, 48 (2), pp.136. �10.1136/jmg.2010.082206�. �hal-00573454�
1 Cohen syndrome diagnosis using whole genome arrays
Nuria Rivera-Brugués
1, Beate Albrecht
3, Dagmar Wieczorek
3, Heinrich Schmidt
4, Thomas Keller
5, Ina Göhring
6, Arif B. Ekici
6, Andreas Tzschach
7, Masoud Garshasbi
7, Kathlen Franke
8, Norman Klopp
9, H.-Erich Wichmann
9,Thomas Meitinger
1,2, Tim M. Strom
1,2, Maja Hempel
1,21
Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany
2
Institute of Human Genetics, Technische Universität München, Munich, Germany
3
Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany
4
Department of Pediatrics, Ludwig-Maximilians-Universität, Munich, Germany
5
Department of Pediatrics, Josefinum Augsburg, Augsburg, Germany
6
Institute of Human Genetics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany
7
Max Planck Institute for Molecular Genetics, Department Human Molecular Genetics, Berlin, Germany
8
Private Clinic B.Prager & A.Junge, Dresden, Germany
9