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Genome-Wide Studies to Identify Rare Variants in BAG3

June 29, 2011 0 Comments

June 30, 2011
6:00 pmto7:00 pm

The June webinar of the free NimbleGen webinar series is talking about
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy >

For further information and registration, please visit the NimbleGen website.

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