- DocumentDeciphering Neurodegenerative Diseases Using Long-Read Sequencinguploaded byShavana Rajkumar
- DocumentGenetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington’s diseaseuploaded byShavana Rajkumar
- DocumentApplications of capillary electrophoresis in DNA mutation analysis of genetic disordersuploaded byShavana Rajkumar
- DocumentAnomalous electrophoretic migration of short oligodeoxynucleotides labelled with 5′-terminal Cy5 dyesuploaded byShavana Rajkumar
- DocumentA simple and rapid analysis of triplet repeat diseases by expand long PCRuploaded byShavana Rajkumar
- DocumentAn update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnosticsuploaded byShavana Rajkumar
- DocumentAmerican College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories, 2014 edition technical standards and guidelines for Huntingtonuploaded byShavana Rajkumar
- DocumentA general method for the detection of large CAG repeat expansions by fluorescent PCRuploaded byShavana Rajkumar
- DocumentTriplet Repeat Primed PCR Simplifies Testing for Huntington Disease (2)uploaded byShavana Rajkumar
- DocumentBIOL 2462 lab 2uploaded byShavana Rajkumar