
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic condition that can lead to life-threatening hemolysis in both children and adults. Early and accurate diagnosis is critical, but identifying G6PD deficiency in newborns and young children isn’t always straightforward—most reference intervals are based on adult values, which don’t necessarily apply to pediatric patients. In this interview, Dr. Kelly Doyle, an ARUP medical director of Special Chemistry, Endocrinology, and Mass Spe...
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An Interview With Dr. Ryan Nelson: Using Pharmacogenetics To Minimize Toxicity With Chemotherapy

An Interview With Ashley Zarling: Navigating the Complex World of Laboratory Billing

An Interview With Dr. Patricia Slev: Laboratory Evaluation of Vaccine-Induced Immunity

An Interview With Dr. Joe Wiencek: Reducing Waste in Clinical Laboratory Testing
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