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Adellgene®: rare diseases diagnosis

Adellgene®: rare diseases diagnosis

Posted on 29 May, 2016 by in Products with no comments

Blackhills Diagnostic Resources offers our product line Adellgene®, based on the fragment analysis for molecular diagnosis of diseases of triplets: Fragile X syndrome, Huntington’s chorea, myotonic dystrophy, Friedreich’s Ataxia, etc. The technology used is based on DNA amplification by PCR, followed by a fluorescent analysis of the fragments obtained.
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