Phenylketonuria, Newborn Screening, Diagnosis & Management
American College of Medical Genetics and Genomics: Phenylalanine hydroxylase deficiency: diagnosis and management guideline,
Genetics in Medicine, January 2, 2014
Genetics in Medicine, January 2, 2014Systematic review: Nutrition management of phenylalanine hydroxylase deficiency.
Rani H. Singh et al. Genetics in Medicine, January 2, 2014
Rani H. Singh et al. Genetics in Medicine, January 2, 2014
What is Phenylketonuria (PKU)? From the National Human Genome Research Institute
From the National Human Genome Research InstitutePhenylalanine hydroxylase deficiency
John J Mitchell, GeneReviews, 2013
CDC Newborn Screening Quality Assurance Program includes phenylketonuria
John J Mitchell, GeneReviews, 2013
CDC Newborn Screening Quality Assurance Program includes phenylketonuria
The political history of PKU: Reflections on 50 years of newborn screening.
Jeffrey P. Brosco and Diane B. Paul, Pediatrics, December 2013
Jeffrey P. Brosco and Diane B. Paul, Pediatrics, December 2013
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