Can anyone verify for me that these were the disorders tested for in the newborn screen in February 2000:
Congenital hypothyroidism
PKU
Biotinidase deficiency
Maple Syrup Urine Disease
Galactosemia
Homocystinuria
Hemoglobinopathies
Congenital hypothyroidism
PKU
Biotinidase deficiency
Maple Syrup Urine Disease
Galactosemia
Homocystinuria
Hemoglobinopathies