192 results on '"Roversi, Gaia"'
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2. Cytogenetically Balanced Reciprocal Translocation Could Hide Molecular Genomic Unbalances: Implications for Foetal Phenotype Correlation.
3. Tubal histopathological abnormalities in BRCA1/2 mutation carriers undergoing prophylactic salpingo-oophorectomy: a case-control study
4. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
5. Molecular signatures of medullary thyroid carcinoma by matrix-assisted laser desorption/ionisation mass spectrometry imaging
6. Genomic Complexity and Complex Chromosomal Rearrangements in Genetic Diagnosis: Two Illustrative Cases on Chromosome 7
7. Insights into the Peritumoural Brain Zone of Glioblastoma: CDK4 and EXT2 May Be Potential Drivers of Malignancy
8. Evaluation of family history in individuals with heterozygous BRCA pathogenic variants diagnosed with breast or ovarian cancer in a single center in Italy
9. 2022-RA-1020-ESGO Family history in BRCA mutation carriers affected by breast and ovarian cancer and its role in identifying subjects at high risk
10. Familiar unbalanced complex rearrangements involving 13 p-arm: description of two cases
11. Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region
12. Tubal histopathological abnormalities in BRCA1/2 mutation carriers undergoing prophylactic salpingo-oophorectomy: a case–control study
13. Solid cell nests of the thyroid gland: morphological, immunohistochemical and genetic features
14. A targeted approach to genetic counseling in breast cancer patients: the experience of an Italian local project
15. An Alternative Approach in Endocrine Pathology Research: MALDI-IMS in Papillary Thyroid Carcinoma
16. Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34 +38 − compartment
17. FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
18. Etude du mobilier céramique
19. Human Chromosome 18 and Acrocentrics: A Dangerous Liaison
20. Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations
21. Evidence for a link between TNFRSF11A and risk of breast cancer
22. The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers
23. Targeted next-generation sequencing appoints C16orf57 as Clericuzio-type poikiloderma with neutropenia gene
24. Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes
25. Genomic and Epigenomic Profile of Uterine Smooth Muscle Tumors of Uncertain Malignant Potential (STUMPs) Revealed Similarities and Differences with Leiomyomas and Leiomyosarcomas
26. Spontaneous chromosomal instability in peripheral blood lymphocytes from two molecularly confirmed Italian patients with Hereditary Fibrosis Poikiloderma: insights into cancer predisposition
27. Additional file 8 of Exploring the link between MORF4L1 and risk of breast cancer
28. Additional file 7 of Exploring the link between MORF4L1 and risk of breast cancer
29. Additional file 16 of Exploring the link between MORF4L1 and risk of breast cancer
30. Additional file 5 of Exploring the link between MORF4L1 and risk of breast cancer
31. Additional file 9 of Exploring the link between MORF4L1 and risk of breast cancer
32. Les amphores régionales en Auvergne (Puy-de-Dome, Allier, Haute-Loire) : typologie et diffusion
33. I materiali
34. Additional file of Exploring the link between MORF4L1 and risk of breast cancer
35. The neural progenitor-restricted isoform of the MARK4 gene in 19q13.2 is upregulated in human gliomas and overexpressed in a subset of glioblastoma cell lines
36. Rothmund–Thomson syndrome and RECQL4 defect: Splitting and lumping
37. Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers
38. Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes. Report of 24 Unrelated Cases
39. Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses
40. Il sistema fognario della città romana di Ostra (Ostra Vetere, An)
41. Exploring the link between MORF4L1 and risk of breast cancer
42. Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa
43. [1] Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa
44. Review of: Carlotta Franceschelli, Pier Luigi Dall’Aglio, Laurent Lamoine (eds). 2017. 'Spazi pubblici e dimensione politica nella città romana: funzioni, strutture, utilizzazione'. Bologna: Bononia University Press
45. Refining the Phenotype of Recurrent Rearrangements of Chromosome 16
46. Rothmund-Thomson syndrome
47. La nascita di Ostra e le fasi costruttive del tempio principale della città
48. L’impianto fognario della città romana di Ostra (Ostra Vetere - AN)
49. Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma
50. Multiple Localization of Endogenous MARK4L Protein in Human Glioma
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