230 results on '"Hanks, Sandra"'
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2. G2: Film & Music: Reviews: Trivial pursuit: Stephen Daldry's preposterous adaptation of the Jonathan Safran Foer novel belittles the impact of 9/11: Extremely Loud & Incredibly Close 1/5 Director: Stephen Daldry. With: Tom Hanks, Sandra Bullock, Thomas Horn, Max von Sydow. 129min. Cert: 12A
3. Molecular, cellular and clinical characterisation of mosaic variegated aneuploidy syndrome
4. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
5. Abstract 4347: A pivotal clinical trial of cResponse, a functional assay for cancer precision medicine
6. Data from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
7. Supplementary Figures 1-5, Table 1 from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
8. Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis
9. Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
10. Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
11. Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
12. Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer
13. Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma
14. Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
15. Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype
16. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome
17. Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
18. Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13. (Report)
19. NSD1 mutations are the major cause of sotos syndrome and occur in some cases of weaver syndrome but are rare in other overgrowth phenotypes
20. Comparative genomic hybridization and BUB1B mutation analyses in childhood cancers associated with mosaic variegated aneuploidy syndrome
21. The gene for juvenile hyaline fibromatosis maps to chromosome 4q21. (Report)
22. DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome
23. Chromosomal instability by mutations in a novel specificity factor of the minor spliceosome
24. Frequency and Heritability of WT1 Mutations in Nonsyndromic Wilmsʼ Tumor Patients: A UK Children’s Cancer Study Group Study
25. Identification of new Wilms tumour predisposition genes: an exome sequencing study
26. The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis
27. Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
28. Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
29. Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
30. Erratum: Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor
31. The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis
32. Mutations in the transcriptional repressor REST predispose to Wilms tumor
33. The ICR1000 UK exome series: a resource of gene variation in an outbred population
34. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour
35. Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
36. Erratum: A genome-wide association study identifies susceptibility loci for Wilms tumor
37. Erratum: A genome-wide association study identifies susceptibility loci for Wilms tumor
38. A genome-wide association study identifies susceptibility loci for Wilms tumor
39. Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
40. Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma
41. Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
42. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
43. Aneuploidy-Cancer Predisposition Syndromes: A New Link between the Mitotic Spindle Checkpoint and Cancer
44. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome
45. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
46. Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.
47. Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.
48. AWT1exon 1 mutation in a child diagnosed with Denys-Drash syndrome.
49. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
50. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
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