| http://www.w3.org/ns/prov#value | - California newborn screening program, a leader in genetic screening tests newborns for 76 genetic disorders including sickle-cell disease and other hemoglobinopathies, primary congenital hypothyroidism, galactosemia (transferase deficiency), biotinidase deficiency, cystic fibrosis (immunoreactive trypsin), amino acid, organic acid, and fatty acid disorders.
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