PerkinElmer scientists in concert with colleagues from the University Hospital of Wales and Cardiff University have developed a new immunoassay screen for Duchenne Muscular Dystrophy.
The Philippines is celebrating the 20th anniversary of newborn screening by announcing a further expansion of the program and its goals.
Sub-Saharan Africa has the highest percentage of births with sickle cell disease. Dr. Russell E. Ware and PerkinElmer are collaborating to train African medical technicians to conduct SCD screening on their own.
Animated cartoon features the benefits of newborn screening for genetic diseases.
Dr. Linh Hoang, Vice President, Neonatal Screening, at PerkinElmer, talks about the challenges, opportunities, and company activities to address the need for newborn screening in India.
Making a statement for safer pregnancies and healthier babies in India.
A couple who lost an infant daughter to a rare metabolic disease is working with PerkinElmer to introduce newborn screening technology to Pakistan.
A global call to action for newborn screening
Genetic Screening Processor will speed testing of millions of babies for genetic disorders.
An extraordinary day in the life of an infant with Maple Syrup Urinary Disease (MSUD).