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Cohen, David

Specific Genetic Disorders and Autism : Clinical Contribution Towards their Identification

Abstract: L'autismo è un disturbo eterogeneo che può rivelare una specifica malattia genetica. Questo articolo descrive diverse malattie genetiche costantemente associate all'autismo (X fragile, sclerosi tuberosa, sindrome di Angelman, duplicazione di 15q11-q13, sindrome di Down, sindrome di San Filippo, disturbi correlati a MECP2, fenilchetonuria, sindrome di Smith-Magenis, delezione 22q13, deficit liasi di adenilosuccinato, sindrome di Cohen e sindrome di Smith-Lemli-Opitz) e propone una strat ...; [read all]
Cover Specific Genetic Disorders and Autism : Clinical Contribution Towards their Identification
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    Description Specific Genetic Disorders and Autism : Clinical Contribution Towards their Identification / Cohen, David; Pichard, Nadège; Tordjman, Sylvie; Baumann, Clarisse; Burglen, Lydie; Excoffier, Elsa; Lazar, Gabriela; Mazet, Philippe; Pinquier, Clément; Verloes, Alain; Héron, Delphine. - Journal of Autism and Developmental Disorders, 2005, 35, 1 ; pp. 103-116
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    • ISSN: 0162-3257
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    ID file 20343
    Permalink https://biblioteca.legadelfilodoro.it/?ids=20343
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    Baumann, Clarisse
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    Burglen, Lydie
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    Excoffier, Elsa
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    Heron, Delphine
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    Lazar, Gabriela
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    Mazet, Philippe
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    Pichard, Nadege
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    Pinquier, Clement
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    Tordjman, Sylvie
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    Verloes, Alain
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    Cohen, David
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