Biology, asked by nishthachhajer503, 1 year ago

It is risk free blood test that detect whether the baby is that increased risk of certain chromosomal abnormalities

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Answered by MiSSiLLuSioN
0
Hello dear ☺️

Here's the answer ⤵️

The Chromosome Laboratory at the Department of Clinical Genetics at Rigshospitalet will be the first in Scandinavia to offer and perform a new genetic screening test for chromosome abnormalities such as D​​own syndrome from 1 September 2015. The test is on a blood sample, which is analysed using an extremely advanced method known as NIPT (Non-Invasive Prenatal Test).​

Hope the given information is helpful ✌️
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