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Efectividad clínica del cribado neonatal de errores congénitos del metabolismo mediante espectrometría de masas en tándem. Parte I: enfermedad de la orina con olor a jarabe de arce, homocistinuria, acidemia glutárica tipo I, acidemia isovalérica y deficiencia de 3-hidroxi-acil-CoA deshidrogenasa de cadena larga110

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