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1. Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

7. Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics

9. The Transcription Factor Encyclopedia

11. Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material

14. 37/#877 Hormonal biomarkers remain prognostic relevant within the molecular classification in endometrial cancer

15. Diagnostic accuracy of mutational analysis along the Müllerian tract to detect ovarian cancer

16. Identification of Fusion Genes and Targets for Genetically Matched Therapies in a Large Cohort of Salivary Gland Cancer Patients

17. GNA11‐mutated Sturge–Weber syndrome has distinct neurological and dermatological features

19. GNA11‐mutated Sturge‐Weber Syndrome has distinct neurologica

20. Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas

21. Additional file 1 of Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material

22. Additional file 3 of Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material

24. High frequency of inactivating tetraspanin CD37 mutations in diffuse large B-cell lymphoma at immune-privileged sites

25. Molecular profiling identifies synchronous endometrial and ovarian cancers as metastatic endometrial cancer with favorable clinical outcome

26. Clonal Relationship Between Lichen Sclerosus, Differentiated Vulvar Intra-epithelial Neoplasia and Non HPV-related Vulvar Squamous Cell Carcinoma

27. Mutational analysis of cervical cytology improves diagnosis of endometrial cancer: A prospective multicentre cohort study

29. Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases

31. ESM_1.docx

33. ESM_3 (figures of immunohistochemical staining)

35. Mutational analysis of cervical cytology improves diagnosis of endometrial cancer: A prospective multicentre cohort study.

37. Correlates of response to anti-PD-1 immune checkpoint blockade (ICB) in mismatch repair proficient (MMRp) and deficient (MMRd) patients (pts) with metastatic castration resistant prostate cancer (mCRPC).

39. Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: A study of 19 cases

40. Profiling of the metabolic transcriptome via single molecule molecular inversion probes

41. BRCA Testing by Single-Molecule Molecular Inversion Probes

42. NovelBRCA1andBRCA2Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas

43. Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags

45. High frequency of inactivating tetraspanin CD37mutations in diffuse large B-cell lymphoma at immune-privileged sites

46. FOXO target gene CTDSP2 regulates cell cycle progression through Ras and p21Cip1/Waf1

48. Novel EWSR1-SMAD3Gene Fusions in a Group of Acral Fibroblastic Spindle Cell Neoplasms

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