Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature

Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature

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Veröffentlicht in:Journal of pediatric genetics 2020, Vol.9 (4), p.270-278
Hauptverfasser: Abarca-Barriga, Hugo H, Trubnykova, Milana, Chavesta-Velásquez, Félix, Barletta-Carrillo, Claudia, Ordoñez-Linares, Marco, Rondón-Abuhadba, Andrea
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container_end_page 278
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container_title Journal of pediatric genetics
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creator Abarca-Barriga, Hugo H
Trubnykova, Milana
Chavesta-Velásquez, Félix
Barletta-Carrillo, Claudia
Ordoñez-Linares, Marco
Rondón-Abuhadba, Andrea
description
doi_str_mv 10.1055/s-0039-3402048
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
title Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature
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