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  1. Germline whole exome sequencing and large-scale replication identifies FANCM as a likely...

    We analyzed whole exome sequencing data in germline DNA from 412 high grade serous ovarian cancer (HGSOC) cases from The Cancer Genome Atlas Project and identified 5,517 genes harboring a predicted deleterious germline coding mutation in at least

    http://iris.ucl.ac.uk/iris/publication/1289179/1

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