Milestone highlights growing adoption of DNA and RNA-informed diagnostics for hereditary cancer and rare disease
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Ambry’s Contributions to MAVEs Support Thousands of Patient Reclassifications and Expand to New Genes
Making Waves: New study published in Nature Communications builds on Ambry’s contributions to MAVE research to deepen understanding of PALB2 and its role in hereditary cancer predisposition.
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Peer-reviewed research highlights the power of proactive reanalysis in rare disease diagnosis.
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