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Cancer Genetics and Cytogenetics|March 1, 1991
Chromosomal characterizations of human nasal and nasopharyngeal cells immortalized by human papillomavirus type 16 DNAM Debiec-Rychter, K Zukowski, C Y Wang, et al.Cancer Genetics and Cytogenetics|May 28, 2008
Malignant myoepithelioma of soft tissue: a case report with cytogenetic findingsZsófia Balogh, Linda Deák, Zoltán SápiCancer Genetics and Cytogenetics|December 11, 2007
FAS -1377 G/A polymorphism and the risk of lymph node metastasis in cervical cancerSokbom Kang, Seung Myung Dong, Sang Soo Seo, et al.Cancer Genetics and Cytogenetics|December 11, 2007
Identification of polymorphisms in the XIAP gene and analysis of association with lung cancer risk in a Korean populationHyo-Gyoung Kang, Su Jeong Lee, Myung Hwa Chae, et al.Cancer Genetics and Cytogenetics|December 11, 2007
TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomasVítor Lima-Ramos, Luís Pacheco-Figueiredo, Sandra Costa, et al.Cancer Genetics and Cytogenetics|December 11, 2007
Determination of ancestral allele for possible human cancer-associated polymorphismsYuichi Maruta, Naoko Okayama, Mikako Hiura, et al.Cancer Genetics and Cytogenetics|December 11, 2007
Methylation of PTCH1, the Patched-1 gene, in a panel of primary medulloblastomasJoel I Pritchard, James M OlsonCancer Genetics and Cytogenetics|December 11, 2007
Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2Catherine Hélias, Stephanie Struski, Carine Gervais, et al.Cancer Genetics and Cytogenetics|December 11, 2007
Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosisMachiko Kawamura, Hidefumi Kaku, Takeshi Taketani, et al.Cancer Genetics and Cytogenetics|June 19, 2008
Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndromeE C B da Costa, F R Vargas, A S Moreira, et al.Pageof 591