HIGHLIGHTS
- who: Fragile X syndrome et al. from the Department of Research on Children with Special Needs, National Research Centre, Cairo, Egypt have published the research work: Simple molecular diagnostic method for Fragile X syndrome in Egyptian patients: Pilot study, in the Journal: (JOURNAL)
- what: The authors aimed to validate an easy and robust methodology for detection of premutation carrier females of FXS and to distinguish between large normal and small premutation alleles which can`t be detected by Southern blot. The authors evaluate the Expand Long Template PCR system (Roche Diagnostics, Mannheim, Germany) in conjunction . . .
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