Abstract
Fluorescence in situ hybridization (FISH) is among the most simple and useful methods for detecting numerical and structural aberration of chromosomes but it requires 12-24 h to complete. We devised a rapid FISH method that can be performed within 2 h. Here we describe the technique, which we have found to be extreme simple and as sensitive and specific as standard FISH, making it highly suitable for clinical use.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Aged, 80 and over
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Allelic Imbalance
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Chromosome Aberrations
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Chromosomes, Human, Pair 1 / genetics
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Chromosomes, Human, Pair 11 / genetics
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Chromosomes, Human, Pair 17 / genetics
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Chromosomes, Human, Pair 18 / genetics
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Colorectal Neoplasms / genetics
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Colorectal Neoplasms / pathology
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Cytodiagnosis*
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Diagnosis, Differential
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Esophageal Neoplasms / genetics
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Esophageal Neoplasms / pathology
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Female
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Humans
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In Situ Hybridization, Fluorescence / methods*
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Male
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Middle Aged
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Neoplasms / genetics
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Neoplasms / pathology*
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Sensitivity and Specificity
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Stomach Neoplasms / genetics
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Stomach Neoplasms / pathology
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Time Factors
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U937 Cells
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Y Chromosome / genetics