Resultados de procura - Evans, D Gareth

Neurofibromatosis type 2 (NF2): A clinical and molecular review por Evans, D Gareth R

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Can the breast screening appointment be used to provide risk assessment and prevention advice? por Evans, D. Gareth, Howell, Anthony

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Family history of breast cancer: Referral guidelines changed after acceptance of 10 minute consultation por Evans, D Gareth, Easton, Douglas

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Breast cancer risk-assessment models por Evans, D Gareth R, Howell, Anthony

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The pathology of familial breast cancer: Clinical and genetic counselling implications of breast cancer pathology por Lalloo, Fiona, Evans, D Gareth R

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PTCH2 is not a strong candidate gene for gorlin syndrome predisposition por Smith, Miriam J., Evans, D. Gareth

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Reduced life expectancy seen in hereditary diseases which predispose to early-onset tumors por Evans, D Gareth R, Ingham, Sarah Louise

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Multifocality in neurofibromatosis type 2 por Evans, D. Gareth R., Stivaros, Stavros M.

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Can manipulation of splicing offer gene therapy possibilities to those with tumour-prone disorders? por Evans, D Gareth R, Wallace, Andrew, Newman, William

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Should unaffected female BRCA2 pathogenic variant carriers be told there is little or no advantage from risk reducing mastectomy? por Evans, D. Gareth, Howell, Sacha J., Howell, Anthony

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Comparison of the frequency of loss‐of‐function LZTR1 variants between schwannomatosis patients and the general population por Deng, Fanxuan, Evans, D. Gareth, Smith, Miriam J.

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Genetic predisposition to peripheral nerve neoplasia: Diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes por Rodriguez, Fausto J., Stratakis, Constantine A., Evans, D Gareth

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Malignant peripheral nerve sheath tumours in inherited disease por Evans, D Gareth R, Huson, Susan M, Birch, Jillian M

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Increased risk of breast cancer in neurofibromatosis type 1: current insights por Howell, Sacha J, Hockenhull, Kimberley, Salih, Zena, Evans, D Gareth

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Exhaustive non-synonymous variants functionality prediction enables high resolution characterization of the neurofibromin architecture por Isakov, Ofer, Wallis, Deeann, Evans, D. Gareth, Ben-Shachar, Shay

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Sporadic implementation of UK familial mammographic surveillance guidelines 15 years after original publication por Evans, D. Gareth, Edwards, Maria, Duffy, Stephen W., Tischkowitz, Marc

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From BRCA1 to Polygenic Risk Scores: Mutation-Associated Risks in Breast Cancer-Related Genes por Woodward, Emma R., van Veen, Elke M., Evans, D. Gareth

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Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer por Ripperger, Tim, Evans, D Gareth, Malkin, David, Kratz, Christian P.

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Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with... por Ripperger, Tim, Evans, D. Gareth, Malkin, David, Kratz, Christian P.

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Basal Cell Carcinomas in Gorlin Syndrome: A Review of 202 Patients por Jones, Elizabeth A., Sajid, Mohammed Imran, Shenton, Andrew, Evans, D. Gareth

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