Rare Chromosome 19p13.3 Deletion Linked to Fatal Infant Heart and Gut Complications
A new case report describes a fatal infant case of 19p13.3 microdeletion syndrome featuring severe cardiomegaly, gastrointestinal complications, and a ...
A new case report describes a fatal infant case of 19p13.3 microdeletion syndrome featuring severe cardiomegaly, gastrointestinal complications, and a ...
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© 2025 Scienmag - Science Magazine