Chromosome 16q22-linked familial AML: Exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms

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• Experimental design. [Word document] [HTML document]
• Table 1: Genes and Primers [Excel document] [HTML document]
• Table 2: Probes for Northern [Excel document] [HTML document]
• Fig.A. RTPCR results [as a JPG] [HTML document]

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