33 results on '"Hanks, Sandra"'
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2. Data from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
3. Data from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
4. Supplementary Figures 1-5, Table 1 from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
5. Supplementary Figures 1-5, Table 1 from Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
6. Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
7. Chromosomal instability by mutations in a novel specificity factor of the minor spliceosome
8. Identification of new Wilms tumour predisposition genes: an exome sequencing study
9. The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis
10. Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
11. Erratum: Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor
12. The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis
13. Mutations in the transcriptional repressor REST predispose to Wilms tumor
14. The ICR1000 UK exome series: a resource of gene variation in an outbred population
15. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour
16. Erratum: A genome-wide association study identifies susceptibility loci for Wilms tumor
17. Erratum: A genome-wide association study identifies susceptibility loci for Wilms tumor
18. A genome-wide association study identifies susceptibility loci for Wilms tumor
19. Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer
20. Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
21. Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma
22. Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis
23. Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy
24. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
25. Comparative genomic hybridization and BUB1B mutation analyses in childhood cancers associated with mosaic variegated aneuploidy syndrome
26. Aneuploidy-Cancer Predisposition Syndromes: A New Link between the Mitotic Spindle Checkpoint and Cancer
27. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome
28. Frequency and Heritability of WT1 Mutations in Nonsyndromic Wilms' Tumor Patients: A UK Children’s Cancer Study Group Study
29. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
30. Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
31. Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease (EDS-VIII) Is a Distinct, Heterogeneous Disorder with One Predisposition Gene at Chromosome 12p13
32. NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes
33. The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21
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