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FISH FOR SEX CHROMOSOME MOSAICISM (TURNER/KLINEFELTER SYNDROME) FROM BLOOD

6,000.00

Fluorescence in situ hybridization (FISH) is a valuable technique for detecting sex chromosome mosaicism, including Turner and Klinefelter syndromes, in blood samples. FISH can identify low-level mosaicism, where some cells have a normal chromosome number while others have an abnormal number, that might be missed by traditional karyotyping.

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Fluorescence in situ hybridization (FISH) is a valuable technique for detecting sex chromosome mosaicism, including Turner and Klinefelter syndromes, in blood samples. FISH can identify low-level mosaicism, where some cells have a normal chromosome number while others have an abnormal number, that might be missed by traditional karyotyping.

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