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iHope Podcast on RareShare

Publication date: 20 Apr 2019

Listen to our latest podcast to learn how Rare Genomics Institute's iHope program helps patients with unknown rare diseases get diagnosed though genomic sequencing in coordination with commercial partners.  Romina Ortiz, Rare Genomics' co-founder and COO, describes the origin of the program, how it is accessed, some of its challenges and how it has successfully helped patients with rare diseases.  Access the podcast from the RareShare website.