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1. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

2. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

3. Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers

4. Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility

5. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

6. Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers

7. Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients

8. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

9. Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect

10. Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

11. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

12. Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

13. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

14. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

15. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

16. Risks of less common cancers in proven mutation carriers with lynch syndrome

17. A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers

18. Breast cancer risk and 6q22.33: Combined results from breast cancer association consortium and consortium of investigators on modifiers of brca1/2

19. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

20. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

21. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

22. Risks of lynch syndrome cancers for msh6 mutation carriers

23. Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

24. A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history

25. Attitude towards pre-implantation genetic diagnosis for hereditary cancer

26. The -148 C/T fibrinogen gene polymorphism and fibrinogen levels in ischaemic stroke: a case-control study

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