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You searched for: Author/Creator Wallace, Andrew J

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1. Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers. Issue 4 (15th January 2021)

3. Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network. Issue 12 (13th March 2020)

4. Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients. Issue 10 (14th August 2015)

5. Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations. Issue 5 (18th November 2020)

6. Confirmation that somatic mutations of beta‐2 microglobulin correlate with a lack of recurrence in a subset of stage II mismatch repair deficient colorectal cancers from the QUASAR trial. Issue 2 (5th July 2019)

7. Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset. Issue 4 (28th January 2011)

8. Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas. Issue 4 (6th October 2014)

9. High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer. Issue 2 (23rd March 2021)