Publication | Closed Access
Newborn screening for congenital hypothyroidism, galactosemia and biotinidase deficiency in Uttar Pradesh, India
38
Citations
18
References
2014
Year
Uttar PradeshInherited Metabolic DiseasePediatricsMaternal HealthCongenital HypothyroidismPrenatal DiagnosisPrenatal TestingBiotinidase DeficiencyMedicine
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