High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy. [electronic resource]
Producer: 20080312Description: 2328-33 p. digitalISSN:- 1090-0535
- Biopsy, Fine-Needle
- Choroid Neoplasms -- genetics
- Chromosomes, Human, Pair 1 -- genetics
- Chromosomes, Human, Pair 3 -- genetics
- Chromosomes, Human, Pair 6 -- genetics
- Chromosomes, Human, Pair 7 -- genetics
- Chromosomes, Human, Pair 9 -- genetics
- Cytogenetic Analysis -- methods
- Gene Expression Profiling -- methods
- Humans
- In Situ Hybridization, Fluorescence -- methods
- Karyotyping -- methods
- Melanoma -- genetics
- Monosomy -- diagnosis
- Oligonucleotide Array Sequence Analysis -- methods
- Polymorphism, Single Nucleotide
- Sensitivity and Specificity
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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