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Beatrix Elmont
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Beatrix Elmont
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Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene
by
Orsolya Nagy
,
Judit Kárteszi
,
Beatrix Elmont
,
Anikó Ujfalusi
Published 2021-08-01
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