Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: a case report.

Maccarini, Stefania; Cipani, Annamaria; Bertini, Valeria; Skripac, Jelena; Salvi, Alessandro; Borsani, Giuseppe; Marchina, Eleonora

Maccarini, Stefania; Cipani, Annamaria; Bertini, Valeria; Skripac, Jelena; Salvi, Alessandro; Borsani, Giuseppe; Marchina, Eleonora.

Afiliação

Maccarini S; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Cipani A; Unit of Child and Adolescent Neuropsychiatry, ASST of Garda, Brescia, Italy.
Bertini V; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Skripac J; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Salvi A; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Borsani G; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Marchina E; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.

Mol Cytogenet ; 13: 23, 2020.

Article em En | MEDLINE | ID: mdl-32582378

Palavras-chave

Array-CGH; CNVs; Gilles de la Tourette syndrome; Intellectual disability; PAR2; Xq28 trisomy

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Ano de publicação: 2020 Tipo de documento: Article

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