Join this NHS webinar on foetal anomaly rapid testing to enhance your knowledge on R21.
In the National Genomic Test Directory, the R21 clinical indication is a rapid test for foetal anomalies with a likely monogenic disorder. The test involves rapid exome sequencing and considers a nationally agreed panel of genes that are known to cause fetal structural anomalies.
This webinar, co-hosted by NHS Central and South Genomics and the North Thames Genomics Laboratory Hub (which perform the test), is for NHS professionals (only) who want to learn more about rapid testing for foetal anomalies.
