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Bio B2BBIONET Corp. 〉FXS Carrier Testing (Genetic Testing)

FXS Carrier Testing (Genetic Testing)


Fragile X Syndrome is one of the most common sex-linked genetic mental retardation diseases.
FMRP for the generation of FMR1. It would affect brain growth and cause mental retardation.


Fragile X Syndrome is one of the most common sex-linked genetic mental retardation diseases.
Fragile X Syndrome is caused by the genetic mutation of FMR1 and abnormal trinucleotide repeat, resulting in abnormal methylation and inability to produce FMRP for the generation of FMR1. It would affect brain growth and cause mental retardation.
Fragile X Syndrome Screening can detect whether the examinees are carriers and understand the risks of the next generation having Fragile X Syndrome. 

We use PCR based technology  based on Triplet Repeat Primed PCR (TP-PCR) design to reliably amplify and detect all alleles including Full Mutations.
Service procedure
3-5c.c of whole blood is collected by ordinary blood drawing and is placed in the purple-capped EDTA blood collection tube. We will extract DNA from this blood sample, carrying out the genetic test directly. The result can be known in 2 weeks.
 
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