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3. Characterization of renal cell carcinoma‐associated constitutional chromosome abnormalities by genome sequencing. Issue 6 (5th February 2020)

8. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification. Issue 9 (13th September 2019)

9. Pathogenic germline variants in patients with features of hereditary renal cell carcinoma: Evidence for further locus heterogeneity. Issue 1 (19th September 2020)

10. Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis. (25th March 2015)