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.

Afiliación

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 en En | MEDLINE | ID: mdl-32582378

Palabras clave

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

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Año: 2020 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google