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Amniotic fluid exosomes (AF-Exos) are pivotal carriers of biological information during fetal development, yet their role in 22q11.2 Deletion Syndrome (22q11.2DS) remains obscure. To elucidate the molecular mechanisms underlying fetal anomalies in 22q11.2DS, we performed DIA Proteomics analysis of A...
ORGANISM(S): Homo Sapiens 
2026-01-21 | PXD073321 |
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