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ReviewDiagnostics (Basel, Switzerland)2025

Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders.

Efthalia Moustakli et al.PubMed ↗Full text ↗Publisher ↗

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13 papers cite it

2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 40722552