Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the <i>FOXP2</i> Gene.

Nagy, Orsolya; Kárteszi, Judit; Elmont, Beatrix; Ujfalusi, Anikó

Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene.

Nagy, Orsolya; Kárteszi, Judit; Elmont, Beatrix; Ujfalusi, Anikó.

Afiliação

Nagy O; Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Kárteszi J; Hospital of Zala County, Zalaegerszeg, Hungary.
Elmont B; Department of Pediatrics, Hospital of Zala County, Zalaegerszeg, Hungary.
Ujfalusi A; Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Front Pediatr ; 9: 664548, 2021.

Article em En | MEDLINE | ID: mdl-34490154

Palavras-chave

7q31 deletion; FOXP2; MLPA; case report; expressive speech disorder

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article