Fluorescence in situ hybridization as a tool to characterize genetic alterations in pancreatic adenocarcinoma
Published in
Pancreas, vol. 39, no. 4, p. 543-544Publication date
2010Keywords
- Adenocarcinoma/diagnosis/*genetics
- *Chromosome Aberrations
- Chromosomes, Human, Pair 17/genetics
- Chromosomes, Human, Pair 18/genetics
- Chromosomes, Human, Pair 8/genetics
- Chromosomes, Human, Pair 9/genetics
- Cyclin-Dependent Kinase Inhibitor p16/genetics
- Humans
- In Situ Hybridization, Fluorescence/*methods
- Pancreatic Neoplasms/diagnosis/*genetics
- Proto-Oncogene Proteins c-myc/genetics
- Reproducibility of Results
- Sensitivity and Specificity
- Smad4 Protein/genetics
- Tumor Suppressor Protein p53/genetics
Citation (ISO format)
GENEVAY-INFANTE, Muriel et al. Fluorescence in situ hybridization as a tool to characterize genetic alterations in pancreatic adenocarcinoma. In: Pancreas, 2010, vol. 39, n° 4, p. 543–544. doi: 10.1097/MPA.0b013e3181bbff44
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Article
Identifiers
- PID : unige:20962
- DOI : 10.1097/MPA.0b013e3181bbff44
- PMID : 20418759
