Case Stories

Unraveling the genomic complexity of common and rare genetic disorders

May 31, 2016
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
April 16, 2015 

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