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

Nagy, OrsolyaKárteszi, JuditElmont, BeatrixUjfalusi, Anikó2021-08-092021-08-092021Frontiers in Pediatrics. -9 (2021), p. 1-8. -Front. Pediatr. - 2296-23602296-2360http://hdl.handle.net/2437/321006Case Report: Expressive Speech Disorder in a Family as Hallmark of 7q31 Deletion Involving the FOXP2 Geneesettanulmányopen access journalhttp://webpac.lib.unideb.hu:8082/ebib/CorvinaWeb?action=cclfind&resultview=long&ccltext=idno+BIBFORM095949OrvostudományokKlinikai orvostudományokszerzőhttp://dx.doi.org/10.3389/fped.2021.6645482022-04-12