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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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-34490154
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Pediatr Year: 2021 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Pediatr Year: 2021 Document type: Article Affiliation country: Country of publication: