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9th International workshop on Fragile X syndrome and X‐linked mental retardation
Authors:Martine Borghgraef  Ted W. Brown  Jamel Chelly  Gene S. Fisch  Ben Hamel  André Hanauer  Didier Lacombe  Ligun Luo  James N. MacPherson  Jean‐Louis Mandel  Claude Moraine  John Mulley  David Nelson  Ben Oostra  Michael Partington  Ger J.A. Ramakers  Hans‐Hilger Ropers  François Rousseau  Charles Schwartz  Peter Steinbach  Claude Stoll  Lisbeth Tranebjaerg  Gillian Turner  Hans Van Bokhoven  Angela Vianna‐Morgante  Laurent Villard  Stephen T. Warren
Affiliation:1. Clinical Genetics Unit/Center for Human Genetics, University Hospital of Leuven, Leuven, Belgium;2. New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York;3. ICGM‐INSERM U129, CHU‐Cochin‐Port‐Royal, Paris, France;4. General Clinical Research Center, Yale University, New Haven, Connecticut;5. Department of Human Genetics, University Hospital Nijmegen, Nijmegen, the Netherlands;6. IGBMC, Illkirch, France;7. Department of Medical Genetics, CHU‐Pellegrin Enfants, Bordeaux, France;8. Biological Sciences, Stanford University, Stanford, California;9. Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury Wiltshire, United Kingdom;10. Service Génétique, Hôpital Bretonneau, Tours, France;11. Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, Australia;12. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas;13. Clinical Genetics Department, Erasmus University, Rotterdam, the Netherlands;14. Newcastle, New South Wales, Australia;15. Neurons and Networks Group, Netherlands Institute for Brain Research, Amsterdam, the Netherlands;16. Max‐Planck Institut für Molekulare Genetik, Berlin‐Dalhem, Germany;17. URGHM, Université Laval Québec, Québec, Canada;18. Center for Molecular Studies, J.C. Self Research Institute, Greenwood Genetics Center, Greenwood, South Carolina;19. Department of Medical Genetics, Universitätsklinikum Ulm, Ulm, Germany;20. Service de Génétique Médicale, Hôpital de Hautepierre, Strasbourg, France;21. Department of Medical Genetics, University Hospital of Tromso, Tromso, Norway;22. Fragile X Department, Hunter Genetics, Waratah, New South Wales, Australia;23. Department de Biologia, Instituto de Biociencias, Universidade de São Paulo, São Paulo, Brazil;24. INSERM U491, Faculté de Médecine La Timone, Marseille, France;25. Department of Biochemistry, Rollins Research Center, HHMI/Emory University, Atlanta, Georgia
Abstract:
Keywords:
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