Sequenced: Using Genetics to Solve Medical Mysteries
Strange symptoms with no clear cause. Medical histories that mystify even the most experienced doctors. Dr. Ian Krantz, Co-Director of CHOP’s Roberts Individualized Medical Genetics…
Strange symptoms with no clear cause. Medical histories that mystify even the most experienced doctors. Dr. Ian Krantz, Co-Director of CHOP’s Roberts Individualized Medical Genetics…
Please Note: This lecture was delivered on January 24, 2020. Per our 3-year review policy in collaboration with the subject matter expert, we’ve decided to…
Please Note: This lecture was delivered on May 24, 2019. Per our 3-year review policy in collaboration with the subject matter expert, we’ve decided to…
Please Note: This lecture was delivered on February 13, 2019. Per our 3-year review policy in collaboration with the subject matter expert, we’ve decided to…
Please Note: This lecture was delivered on July 20, 2018. Per our 3-year review policy in collaboration with the subject matter expert, we’ve decided to…
Noura S. Abul-Husn, MD, PhD is Associate Professor of Medicine and Genetics, founding Chief of the Division of Genomic Medicine in the Department of Medicine,…
Individuals and families continue to face barriers in diagnosis and coordinated management of the complex conditions that arise as a consequence of leukodystrophy. This virtual…
Both targeted and next-generation sequencing have increasing relevance in the diagnosis, prognosis/risk stratification and therapies for solid tumors. In particular, identification of oncogenetic drivers through…
Congenital disorders of glycosylation (CDG) are a large group of rare genetic disorders that affect the addition of sugar building blocks, called glycans, to proteins…
This webinar provides information on the current diagnostic and multi-disciplinary disease management practices for Beckwith-Wiedemann Syndrome (BWS), including a review of a newly published clinical…