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Newborn screening compared to clinical identification of biochemical genetic disorders.
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Newborn screening compared to clinical identification of biochemical genetic disorders.
Newborn screening compared to clinical identification of biochemical genetic disorders. J Inherit Metab Dis. 2002 Nov; 25(7):599-600.
View in:
PubMed
subject areas
Adolescent
Biotinidase Deficiency
Child
Child, Preschool
Galactosemias
Homocystinuria
Humans
Infant
Infant, Newborn
Maple Syrup Urine Disease
Metabolism, Inborn Errors
Neonatal Screening
authors with profiles
Michael E. Msall