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A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci.

Screening of referrals for the mutations associated with the fragile X syndrome constitutes a significant workload in many genetics laboratories. Since the great majority of these referrals will be negative, there is a need for a rapid and inexpensive screening test. We have developed an assay which...

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Bibliografiske detaljer
Main Authors: Wang, Q, Green, E, Bobrow, M, Mathew, C G
Format: Artigo
Sprog:Inglês
Udgivet: 1995
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050311/
https://ncbi.nlm.nih.gov/pubmed/7783163
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