Episodes
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
Published 10/15/21
September: Team of experts creates ACMG’s first evidence-based clinical guideline recommending exome or genome sequencing for pediatric patients with congenital anomalies or intellectual disability
Published 10/15/21
August: Diagnosing the undiagnosed: Genetic testing identifies the underlying causes of kidney disease
Published 10/15/21
July: Artificial intelligence may provide a timely diagnosis for Fragile X syndrome
Published 10/15/21
June: Universal newborn screening to identify pediatric cancer predisposition – could it work?
Published 10/15/21
May: The implementation of clinical genomic DNA methylation testing in patients with rare disorders
Published 10/15/21
February: Targeted exome sequencing for second-tier newborn screening tests: technology to scale
Published 10/15/21
April: Increasing access to genomic medicine in diverse communities: What shapes Latinx perspectives on health care incorporating genomics?
Published 10/15/21
March: Turning principles into policy: Combating systemic racism in genetics and genomics publications
Published 10/15/21
January: Is newborn screening for metachromatic leukodystrophy coming soon?
Published 10/15/21
December: Elamipretide: A treatment for Barth syndrome
Published 10/15/21
November: Exploring a genotype-first approach for genetic variants that influence cardiac diseases
Published 10/15/21
October: Online Access to Down syndrome Health-Care Tool
Published 10/15/21
September: How to overcome barriers and meaningfully engage Alaska Native tribes and tribal health organizations in genomic research
Published 10/15/21
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