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Click on one of the conditions below to view & print the associated Physician Action Sheet.
3-Methylcrotonyl-CoA carboxylase deficiency
Amino acid disorders
Fatty acid oxidation disorders
D/G galactosemia & other galactosemia variants
Medium chain acyl-CoA dehydrogenase deficiency (MCADD)
Maple syrup urine disease (MSUD)
Organic acid disorders
ACMG newborn screening ACT sheets (select "Resources," then click on "ACT Sheets")
National Library of Medicine's Genetics Home Reference
National Newborn Screening & Genetics Resource Center
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