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Making Sense of Our Genes: A BIG conversation with Aarin A Williams, MS, LCGC and Dr. Loydie A. Jerome-Majewska, PhD

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Manage episode 311567591 series 3143719
Content provided by Skype A Scientist. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Skype A Scientist 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.

Aarin A Williams, MS, LCGC
Licensed Certified Genetic Counselor
MS Human Genetics and Genetic Counseling, Stanford University. BS Biology, Howard University.
Aarin currently practices prenatal, cancer and general genetics at Kaiser Permanente Southern California.
Loydie A. Jerome-Majewska, PhD
Ph.D. Columbia University, Post-doc: Sloan Kettering Institute, Associate Professor at McGill University, Depts of Pediatrics, Human Genetics and Anatomy and Cell Biology.
Dr. Jerome-Majewska studies the genetic and molecular basis of abnormal organ development in 22q11.2 deletion syndrome and spliceosomopathies.

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92 episodes

Artwork
iconShare
 
Manage episode 311567591 series 3143719
Content provided by Skype A Scientist. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Skype A Scientist 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.

Aarin A Williams, MS, LCGC
Licensed Certified Genetic Counselor
MS Human Genetics and Genetic Counseling, Stanford University. BS Biology, Howard University.
Aarin currently practices prenatal, cancer and general genetics at Kaiser Permanente Southern California.
Loydie A. Jerome-Majewska, PhD
Ph.D. Columbia University, Post-doc: Sloan Kettering Institute, Associate Professor at McGill University, Depts of Pediatrics, Human Genetics and Anatomy and Cell Biology.
Dr. Jerome-Majewska studies the genetic and molecular basis of abnormal organ development in 22q11.2 deletion syndrome and spliceosomopathies.

  continue reading

92 episodes

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