How Personalized Genetic Testing for Medication Metabolism May Reduce Problems with Medications for People with Cystic Fibrosis
In-depth examination of the CFTR gene finds more disease-causing genetic changes than conventional clinical genetic testing
Presentation of two siblings with CF born to a mother with CF taking Trikafta (Kaftrio) throughout both pregnancies. A baby boy has normal vas deferens after birth.
Lung function and imaging outcomes in children with cystic fibrosis diagnosed after newborn screening
