Breastcancer-genetics
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- 2018
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Mark
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant : Breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
- Contribution to journal › Article
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Mark
The applicability of the translated Edmonton Symptom Assessment System : revised [ESAS-r] in Swedish palliative care
- Contribution to journal › Letter
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Mark
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication
- Contribution to journal › Article
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Mark
Increasing the Elective Endovascular to Open Repair Ratio of Popliteal Artery Aneurysm
- Contribution to journal › Article
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Mark
Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative
- Contribution to journal › Article
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Mark
Bridging gaps in everyday life - a free-listing approach to explore the variety of activities performed by physiotherapists in specialized palliative care
- Contribution to journal › Article
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Mark
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
- Contribution to journal › Article
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Mark
Bereavement stressors and psychosocial well-being of young adults following the loss of a parent – A cross-sectional survey
- Contribution to journal › Article
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Mark
A translational effort to identify prognostic and predictive biomarkers in pancreatic cancer among RBM3-regulated genes
- Contribution to conference › Poster
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Mark
Similarities and Differences of Blood N-Glycoproteins in Five Solid Carcinomas at Localized Clinical Stage Analyzed by SWATH-MS
- Contribution to journal › Article
