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

3. Co-developing Indigenous seasonal calendars to support 'healthy Country, healthy people' outcomes. (April 2019)

4. Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non‐syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma. (6th April 2013)

5. Meeting abstracts from the 64th British Thyroid Association Annual Meeting. Issue 1 (February 2017)

6. Penetrance estimates for BRCA1, BRCA2 (also applied to Lynch syndrome) based on presymptomatic testing: a new unbiased method to assess risk?. Issue 7 (26th February 2018)

7. Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs). Issue 11 (24th April 2019)