Case Stories
Unraveling the genomic complexity of common and rare genetic disorders
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Unraveling the genomic complexity of common and rare genetic disorders: NGS bioinformatics for the discovery of causal variants in sensorineural hereditary hearing loss and various rare conditions
Presented by Rajini R. Haraksingh, Ph.D., Postdoctoral fellow, Stanford University and Vice Precident, Rare Genomics Institute
Presented by Rajini R. Haraksingh, Ph.D., Postdoctoral fellow, Stanford University and Vice Precident, Rare Genomics Institute
April 16, 2015
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