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A rare encounter: Navigating airway challenges in Van den Ende-Gupta syndrome.
First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende-Gupta and 22q11.2 Deletion Syndromes.
📖 RevisãoInteraction mechanism of lipid metabolism remodeling, oxidative stress, and immune response mediated by Epinephelus coioides SRECII.
🥈 ObservacionalExploring scavenger receptor class F member 2 and the importance of scavenger receptor family in prediagnostic diseases.
Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.