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Episode 18 — Connecting the dots in the network of rare
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Manage episode 413262846 series 2136231
Content provided by Rare in Common and Cambridge BioMarketing. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare in Common and Cambridge BioMarketing or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
In this episode recorded at the American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting, hear from 2 experts in the field of genetics. First, Dr. George Diaz discusses his role as a medical geneticist and pediatrician, the value of connecting families affected by rare diseases, and the impact technological advancements have made in his field. Next, Dr. Katy Phelan shares highlights of her career as a laboratory geneticist—including her discovery of a rare deletion syndrome. She explains why when patients connect, it helps their families and improves her research and understanding of the disease.
…
continue reading
29 episodes
MP3•Episode home
Manage episode 413262846 series 2136231
Content provided by Rare in Common and Cambridge BioMarketing. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare in Common and Cambridge BioMarketing or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
In this episode recorded at the American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting, hear from 2 experts in the field of genetics. First, Dr. George Diaz discusses his role as a medical geneticist and pediatrician, the value of connecting families affected by rare diseases, and the impact technological advancements have made in his field. Next, Dr. Katy Phelan shares highlights of her career as a laboratory geneticist—including her discovery of a rare deletion syndrome. She explains why when patients connect, it helps their families and improves her research and understanding of the disease.
…
continue reading
29 episodes
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