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521032
521032
http://dx.doi.org/10.1086/521032
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes
P356
Q36492194-C3CDAED0-2A4E-4129-A142-C2B7BC64EAEA
P356
521032
http://dx.doi.org/10.1086/521032