Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

Author:

Becker Jessica,Czamara Darina,Scerri Tom S,Ramus Franck,Csépe Valéria,Talcott Joel B,Stein John,Morris Andrew,Ludwig Kerstin U,Hoffmann PerORCID,Honbolygó Ferenc,Tóth Dénes,Fauchereau Fabien,Bogliotti Caroline,Iannuzzi Stéphanie,Chaix Yves,Valdois Sylviane,Billard Catherine,George Florence,Soares-Boucaud Isabelle,Gérard Christophe-Loïc,van der Mark Sanne,Schulz Enrico,Vaessen Anniek,Maurer Urs,Lohvansuu Kaisa,Lyytinen Heikki,Zucchelli Marco,Brandeis Daniel,Blomert Leo,Leppänen Paavo HT,Bruder Jennifer,Monaco Anthony P,Müller-Myhsok Bertram,Kere Juha,Landerl Karin,Nöthen Markus M,Schulte-Körne Gerd,Paracchini Silvia,Peyrard-Janvid Myriam,Schumacher Johannes

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference49 articles.

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2. Shaywitz SE, Shaywitz BA, Fletcher JM, Escobar MD : Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study. JAMA 1990; 264: 998–1002.

3. Shaywitz SE, Fletcher JM, Holahan JM et al: Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence. Pediatrics 1999; 104: 1351–1359.

4. ICD-10-GM Version 2008: Internationale statistische Klassifikation der Krankheiten und verwandter Gesundheitsprobleme, 10; Revision - German Modification -; Kapitel V: 192.

5. American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders. Washington, DC: American Psychiatric Association, 2000 4th edn. Text Revision, pp 51-52.

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