Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing
C. Eric Freitag, William R. Sukov, Alan H. Bryce, Jamie V. Berg, Chad Vanderbilt, Wei Shen, James B. Smadbeck, Patricia T. Greipp, Rhett P. Ketterling, Robert B. Jenkins, Loren Herrera-Hernandez, Brian A. Costello, R. Houston Thompson, Stephen A. Boorjian, Bradley C. Leibovich, Rafael E. Jiménez, Stephen J. Murphy, George Vasmatzis, John C. Cheville, Sounak Gupta
Topics & Concepts
Fluorescence in situ hybridizationPolysomyIsochromosomeBiologyChromosome 12Germ cell tumorsChromosomeKaryotypePathologyGeneticsMedicineGeneChemotherapyTesticular diseases and treatmentsCholangiocarcinoma and Gallbladder Cancer StudiesSarcoma Diagnosis and Treatment