Phenylalanine hydroxylase deficiency: diagnosis and management guideline
Jerry Vockley(Pittsburgh Public Schools), Susan A. Berry(University of Minnesota), Dianne M. Frazier(University of North Carolina at Chapel Hill), Wendy E. Smith(Maine Medical Center), Nancy Braverman(McGill University), John J. Mitchell(University of North Carolina at Chapel Hill), Barry H. Thompson(American College of Financial Services), Hans C. Andersson(Tulane University), Barbara K. Burton(Women & Children's Hospital of Buffalo), Kevin M. Antshel(Syracuse University)
Cited by 718
Related Papers
Cockayne syndrome: Review of 140 cases
|American Journal of Medical Genetics|1992|807
Effects of Diet and Physical Activity Interventions on Weight Loss and Cardiometabolic Risk Factors in Severely Obese Adults
|JAMA|2010|554
Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders
|New England Journal of Medicine|2007|355
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
|Genetics in Medicine|2006|269