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Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.
Sumner K, Hubley L, Pont-Kingdon G, Mitchell S, Wayman T, Wilson A, Meadows C, Elenitoba-Johnson K, Pattison D, Dobrowolski S, Best H, Lyon E. Sumner K, et al. Among authors: wilson a. Genet Test Mol Biomarkers. 2012 Jul;16(7):656-60. doi: 10.1089/gtmb.2011.0204. Epub 2012 Feb 24. Genet Test Mol Biomarkers. 2012. PMID: 22364140
Diagnostic utility of microsatellite genotyping for molar pregnancy testing.
Furtado LV, Paxton CN, Jama MA, Tripp SR, Wilson AR, Lyon E, Jarboe EA, Thaker HM, Geiersbach KB. Furtado LV, et al. Among authors: wilson ar. Arch Pathol Lab Med. 2013 Jan;137(1):55-63. doi: 10.5858/arpa.2012-0047-OA. Arch Pathol Lab Med. 2013. PMID: 23276175 Free article.
SPRED 1 mutations in a neurofibromatosis clinic.
Muram-Zborovski TM, Stevenson DA, Viskochil DH, Dries DC, Wilson AR, Rong Mao. Muram-Zborovski TM, et al. Among authors: wilson ar. J Child Neurol. 2010 Oct;25(10):1203-9. doi: 10.1177/0883073809359540. Epub 2010 Feb 22. J Child Neurol. 2010. PMID: 20179001 Free PMC article.
8,958 results