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FISH FOR PATAU SYNDROME/TRISOMY 13

5,500.00

FISH (Fluorescence In Situ Hybridization) is a molecular cytogenetic technique used to detect Trisomy 13 (Patau Syndrome) by identifying an extra copy of chromosome 13 in cells. This test is valuable in prenatal screening and diagnosis, providing rapid results for informed decision-making regarding pregnancy management.

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FISH (Fluorescence In Situ Hybridization) is a molecular cytogenetic technique used to detect Trisomy 13 (Patau Syndrome) by identifying an extra copy of chromosome 13 in cells. This test is valuable in prenatal screening and diagnosis, providing rapid results for informed decision-making regarding pregnancy management.

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