MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients : hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-12-02
著者
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Dhanjal Seema
Department Of Biological Sciences University Of Warwick
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Esposito Maurizio
International Institute Of Genetics And Biophysics
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Filippini Francesco
Dipartimento Di Biologia Universita Di Padova
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HULTEN Maj
Department of Biological Sciences, University of Warwick
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Rossi Valeria
Dipartimento Di Biologia Universita Di Padova
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Kerr Alison
Academic Centre Glasgow University Department Of Psychological Medicine Gartnavel Royal Hospital
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Hulten Maj
Department Of Biological Sciences University Of Warwick
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Hayek Giuseppe
Neuropsichiatria Infantile Policlinico Le Scotte
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VACCA Marcella
International Institute of Genetics and Biophysics
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BUDILLON Alberta
International Institute of Genetics and Biophysics
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RAGIONE Floriana
International Institute of Genetics and Biophysics
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BONIS Maria
International Institute of Genetics and Biophysics
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MERCADANTE Grazia
International Institute of Genetics and Biophysics
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MANZATI Elisa
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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GUALANDI Francesca
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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BIGONI Stefania
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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TRABANELLI Cecilia
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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PINI Giorgio
Servizio di Neuropsichiatria Infantile, U. O.
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CALZOLARI Elisa
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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FERLINI Alessandra
Dipartimento di Medicina Sperimentale e Diagnostica, Universita di Ferrara
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MELONI Ilaria
Genetica Medica, Policlinico Le Scotte, Universita di Siena
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ZAPPELLA Michele
Neuropsichiatria Infantile, Policlinico Le Scotte
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RENIERI Alessandra
Genetica Medica, Policlinico Le Scotte, Universita di Siena
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URSO Michele
International Institute of Genetics and Biophysics
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MACDONALD Fiona
Regional Genetics Services, Birmingham
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Pini Giorgio
Servizio Di Neuropsichiatria Infantile U. O.
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Manzati Elisa
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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Meloni Ilaria
Genetica Medica Policlinico Le Scotte Universita Di Siena
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Macdonald Fiona
Regional Genetics Services Birmingham
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Calzolari Elisa
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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Bigoni Stefania
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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Renieri Alessandra
Medical Genetics Department Of Molecular Biology University Of Siena
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Renieri Alessandra
Genetica Medica Policlinico Le Scotte Universita Di Siena
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Zappella Michele
Neuropsichiatria Infantile Policlinico Le Scotte
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Ferlini Alessandra
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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Gualandi Francesca
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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Trabanelli Cecilia
Dipartimento Di Medicina Sperimentale E Diagnostica Universita Di Ferrara
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ZAPPELLA Michele
Child Neuropsychiatry, Versilia Hospital
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Hayek Giuseppe
Infantile Neuropsychiatry Siena General Hospital
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Zappella Michele
Child Neuropsychiatry Versilia Hospital
関連論文
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- MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients : hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region
- Clinical and molecular characterization of Italian patients affected by Cohen syndrome
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