Tonya L. Di Sera

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Michael T. Parsons1
Amanda B. Spurdle1
David E. Goldgar1
1Michael T. Parsons
1Amanda B. Spurdle
1David E. Goldgar
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Clinical mutation screening of the cancer susceptibility genes BRCA1 and BRCA2 generates many unclassified variants (UVs). Most of these UVs are either rare missense substitutions or nucleotide substitutions near the splice junctions of the protein coding exons. Previously, we developed a quantitative method for evaluation of BRCA gene UVs-the "integrated(More)
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