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Andrea Rondón-Abuhadba
Andrea Rondón-Abuhadba
Medicine
deletion syndrome
Genetics
Gene
FOXP1
2
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2024
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Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature
2020
Journal of pediatric genetics
Hugo H. Abarca-Barriga
Milana Trubnykova
Félix Chavesta Velásquez
Claudia Barletta-Carrillo
Marco Ordoñez-Linares
Andrea Rondón-Abuhadba
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Prácticas de alimentación complementaria, características sociodemográficas y su asociación con anemia en niños peruanos de 6-12 meses
2019
Eddy López Huamanrayme
Noe Israel Atamari Anahui
Marilyn Carmen Rodriguez-Camino
Mayu Gabriel Mirano-Ortiz-de-Orue
Andrea Belen Quispe-Cutipa
Andrea Rondón-Abuhadba
Cesar Johan Pereyra Victorio
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