Primary renal neuroblastoma.

Abstract

sequencing, which possesses the best resolution and is the gold standard for mutation detection. Even SNP arrays need Sanger sequencing data for final validation. Using Sanger sequencing, we found that an AT/RT case possesses a C-insertion point mutation in the coding region of the INI1 gene, and the INI1 gene of other cases examined remained unchanged (Fig… (More)
DOI: 10.1097/PAS.0b013e318264bdf1

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