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QF-PCR rapid aneuploidy screening for chromosomes 13, 18, 21, X and Y and the muration ΔF508 in cystic fibrosis

 

QF-PCR rapid aneuploidy screening for chromosomes 13, 18, 21, X and Y and the muration ΔF508 in cystic fibrosis: this test screens for the 3 most common trisomies found prenatally (chromosomes 13, 18 and 21) and will therefore exclude Edwards, Patau and Down syndromes. It will also give you the sex of your baby and screen for any sex chromosome abnormalities, such as Turner and Kleinfelter syndromes. We also screen for the most common mutation in cystic fibrosis, ΔF508. The result of this test is usually available within 24 hours.

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Molecular profile of a female foetus with trisomy 21

 

 
   
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