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Tag: Clinical Genome Services

Rady Children’s Institute for Genomic Medicine is excited to announce that the current version of our rWGS/urWGS test is now validated to include identification of repeat expansions in the PHOX2B gene, associated with Congenital Central Hypoventilation Syndrome (CCHS), and in the DMPK gene, associated with Myotonic Dystrophy Type 1 (DM1).
Here at Rady Children's Institute for Genomic Medicine®, we're known for our rapid turnaround on tests. Our aim with this blog is to provide you with quick, speedy updates on things relevant to our core work: clinical genomic services, lab tests, rWGS reimbursement, and more. Stay tuned for more.

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