Guidelines for reporting clinical features in cases with MECP2 mutations
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概要
- 論文の詳細を見る
- 2001-07-01
著者
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Nomura Yoshiko
Segawa Neurological Clinic For Children
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SEGAWA Masaya
Segawa Neurological Clinic for Children
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YAMASHITA Yushiro
Department of Pediatrics and Child Health, Kurume University School of Medicine
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Yamashita Yushiro
Department Of Pediatrics & Child Health Kurume University School Of Medicine
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ARMSTRONG Dawna
Department of Pathology, Baylor College of Medicine
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Esposito Maurizio
Cnr Institute Of Genetics And Biophysics Stanford University School Of Medicine
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Naidu Sakkubai
Kennedy Institute
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KERR Alison
Department of Psychological Medicine, Gartnavel Royal Hospital
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ANVRET Maria
Karolinska Institute
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BELICHENKO Pavel
Brain Research Institute
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BUDDEN Sarojini
Oregon Health Sciences University
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CASS Hilary
Great Ormond Street Hospitals
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CHRISTODOULOU John
Department of Paediatrics & Child Health, Children's Hospital at Westmead
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CLARKE Angus
Department of Medical Genetics, University of Wales College of Medicine
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ELLAWAY Carolyn
Department of Paediatrics & Child Health, Children's Hospital at Westmead
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FRANCKE Uta
Howard Hughes Medical Institute, Stanford University School of Medicine
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HULTEN Maj
Department of Biological Sciences, University of Warwick
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JULU Peter
Central Middlesex Hospital
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LEONARD Helen
TVW Telethon Institute for Child Health Research and Disability Services Commission
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SCHANEN Carolyn
UCLA School of Medicine, Department of Human Genetics
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WEBB Tessa
Department of Clinical Genetics, Birmingham Maternity Hospital
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ENGERSTROM Ingegerd
Rett Centre
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Kerr Alison
Department Of Psychological Medicine Gartnavel Royal Hospital
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Hulten Maj
Department Of Biological Sciences University Of Warwick
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Webb Tessa
Department Of Clinical Genetics Birmingham Maternity Hospital
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Francke Uta
Howard Hughes Medical Institute Stanford University School Of Medicine
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Kerr Alison
Department Of Psychological Medicine Academic Centre Gartnavel Royal Hospital
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Clarke Angus
Department Of Medical Genetics University Of Wales College Of Medicine
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Leonard Helen
Centre For Child Health Research The University Of Western Australia
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Nomura Yoshiko
Segawa Neurologic Clinic For Children
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Armstrong Dawna
Department Of Pathology Baylor College Of Medicine
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Schanen Carolyn
Ucla School Of Medicine Department Of Human Genetics
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Ellaway Carolyn
Western Sydney Genetics Program Royal Alexandra Hospital For Children
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Segawa Masaya
Segawa Neurologic Clinic For Children
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Ellaway Carolyn
Department Of Paediatrics & Child Health Children's Hospital At Westmead
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CHRISTODOULOU John
Western Sydney Genetics Program, Royal Alexandra Hospital for Children
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Christodoulou John
Western Sydney Genetics Program Royal Alexandra Hospital For Children
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- Preface
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- Guidelines for reporting clinical features in cases with MECP2 mutations, by Alison Kerr and an international group
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