MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients
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概要
- 論文の詳細を見る
- 2006-06-01
著者
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Smeets Eric
Department Of Clinical Genetics University Hospital Maastricht
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Smeets Eric
Department Of Clinical Genetics Academic Hospital Maastricht
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Schrander-stumpel Connie
Department Of Clinical Genetics University Hospital Maastricht
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Schrander-stumpel Connie
Department Of Clinical Genetics Academic Hospital Maastricht
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MOOG Ute
Department of Clinical Genetics, University Hospital Maastricht
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VAN ROOZENDAAL
Department of Clinical Genetics, University Hospital Maastricht
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TSERPELIS Demis
Department of Clinical Genetics, University Hospital Maastricht
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DEVRIENDT Koen
Center for Human Genetics, University Hospital Gasthuisberg, University of Leuven
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VAN BUGGENHOUT
Center for Human Genetics, University Hospital Gasthuisberg, University of Leuven
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FRIJNS Jean-Pierre
Department of Clinical Genetics, University Hospital Maastricht
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Moog Ute
Department Of Clinical Genetics University Hospital Maastricht
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Devriendt Koen
Center For Human Genetics University Hospital Gasthuisberg University Of Leuven
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Van Roozendaal
Department Of Clinical Genetics University Hospital Maastricht
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Van Buggenhout
Center For Human Genetics University Hospital Gasthuisberg University Of Leuven
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Tserpelis Demis
Department Of Clinical Genetics University Hospital Maastricht
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Frijns Jean-pierre
Department Of Clinical Genetics University Hospital Maastricht
関連論文
- Management of a severe forceful breather with Rett Syndrome using carbogen
- The development of visual- and auditory processing in Rett syndrome : An ERP study
- MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients