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Why should you participate: Karyotype analysis helps in the diagnosis of congenital chromosome abnormalities including aneuploidy, large structural abnormalities and balanced rearrangements. Chromosome microarray is recommended as the first-tier test to detect clinically relevant gains or losses of chromosomal material for individuals with multiple anomalies not specific to well-delineated genetic syndromes, individuals with apparently non-syndromic developmental delay or intellectual disability and individuals with autism spectrum disorders.

With advent of Chromofic Karyoarray, you will get to know when power of these test combined all together in one test, how it offers a complete picture for diagnosis and treatment of a patient.

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Launching Chromofic Karyoarray: A Powerful Combination of Karyotype & Microarray

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