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Chromosomal Breakage Study for Fanconi Anemia (DEB)
A specialized genetic assay to diagnose Fanconi anemia by measuring chromosomal sensitivity to breakage, enabling early detection and timely medical intervention to improve patient outcomes and support clinical management.
An advanced cytogenetic assay using Diepoxybutane (DEB) to evaluate chromosomal stability. It is the gold standard for diagnosing Fanconi anemia and assessing genetic risks associated with bone marrow failure.
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