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ANEUPLOIDY FISH (13,18,21,X & Y)

8,630.00

Aneuploidy FISH (13, 18, 21, X & Y) is a prenatal test that uses fluorescence in situ hybridization (FISH) to detect numerical abnormalities in chromosomes 13, 18, 21, X, and Y. These abnormalities can indicate conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13), and sex chromosome aneuploidies like Turner syndrome (Monosomy X). The test is typically performed on amniotic fluid or chorionic villus samples.

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Description

Aneuploidy FISH (13, 18, 21, X & Y) is a prenatal test that uses fluorescence in situ hybridization (FISH) to detect numerical abnormalities in chromosomes 13, 18, 21, X, and Y. These abnormalities can indicate conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13), and sex chromosome aneuploidies like Turner syndrome (Monosomy X). The test is typically performed on amniotic fluid or chorionic villus samples.

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