High acceptance of an early dyslexia screening test involving genetic analyses in Germany.

Wilcke, Arndt; Müller, Bent; Schaadt, Gesa; Kirsten, Holger; Boltze, Johannes

Wilcke, Arndt; Müller, Bent; Schaadt, Gesa; Kirsten, Holger; Boltze, Johannes.

Afiliação

Wilcke A; Department of Cell Therapy, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Leipzig, Germany.
Müller B; Translational Centre for Regenerative Medicine (TRM), Universität Leipzig, Leipzig, Germany.
Schaadt G; Department of Cell Therapy, Fraunhofer Institute for Cell Therapy and Immunology (IZI), Leipzig, Germany.
Kirsten H; Department of Neuropsychology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Boltze J; Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany.

Eur J Hum Genet ; 24(2): 178-82, 2016 Feb.

Article em En | MEDLINE | ID: mdl-26036858

Assuntos

Dislexia/diagnóstico; Testes Genéticos; Criança; Pré-Escolar; Dislexia/epidemiologia; Dislexia/genética; Eletroencefalografia; Feminino; Alemanha/epidemiologia; Humanos; Masculino; Pais; Fonética; Leitura

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Dislexia Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2016 Tipo de documento: Article

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