Abstract
On April 6, 2012, the Centers for Disease Control and Prevention (CDC) published recommendations for good laboratory practices that address the quality-management needs of biochemical genetic testing and newborn screening (1). The CDC recommendations were developed on the basis of the recommendations and input of 3 federal advisory committees (the Clinical Laboratory Improvement Advisory Committee; the Secretary's Advisory Committee on Genetics, Health, and Society; and …
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
