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Molecular assay reagents intended to identify gene variants associated with Fanconi anemia, a condition leading to bone marrow failure, physical abnormalities, and an increased risk of certain cancers. Genetic variants at multiple loci have been associated with Fanconi anemia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Fanconi anemia-associated loci simultaneously.
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