Andrea Rondón-Abuhadba
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5CO-AUTHORS

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Publications (1)
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|Aug 09, 2020
Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the <i>FOXP1</i> Gene: Review of the Literature.Hugo H Abarca-Barriga, Milana Trubnykova, Félix Chavesta-Velásquez
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