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  1. No Access

    Article

    Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics

    This nationwide study assessed the impact of Lynch syndrome-related risk management guidelines on clinicians’ recommendations of risk management strategies to carriers of pathogenic variants in mismatch repair...

    B. Meiser, R. Kaur, J. Kirk, A. Morrow, M. Peate, W. K. T. Wong… in Familial Cancer (2020)

  2. No Access

    Article

    Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same

    Many cancer predisposition syndromes are preceded or accompanied by a range of typical skin signs. Gorlin syndrome is a rare multisystem inherited disorder which can predispose to basal cell carcinomas (BCCs),...

    A. J. Huq, M. Walsh, B. Rajagopalan, M. Finlay, A. H. Trainer, F. Bonnet… in Familial Cancer (2018)

  3. Article

    Open Access

    Tumour morphology predicts PALB2 germline mutation status

    Population-based studies of breast cancer have estimated that at least some PALB2 mutations are associated with high breast cancer risk. For women carrying PALB2 mutations, knowing their carrier status could be u...

    Z L Teo, E Provenzano, G S Dite, D J Park, C Apicella… in British Journal of Cancer (2013)

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