ArticleMolecular genetics & genomic medicine2025

Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification.

Thania Alejandra Aguayo-Orozco et al.PubMed ↗Full text ↗Publisher ↗

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