Digital multiplex ligation-dependent probe amplification identifies exon-level copy number variants in patients with suspected hereditary cancer and negative next-generation sequencing results

Mol Biol Rep. 2026 Feb 16;53(1):392. doi: 10.1007/s11033-026-11541-3.
No abstract available

Keywords: CDKN2A; CNV; Digital MLPA; Hereditary cancer; Lynch syndrome; MLH1; PMS2.