Molecular bases of congenital hypothyroidism

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Pinzón-Serrano, Estefanía; Morán-Barroso, Verónica; Coyote-Estrada, Ninel;
(2006)
  • Publisher: Instituto Nacional de Salud, Hospital Infantil de México Federico Gómez
  • Subject: mutations | mutaciones | PAX8 | dyshormonogenesis | NKX2.1 | FOXE1 | dishormonogénesis | Congenital hypothyroidism | Hipotiroidismo congénito

Las alteraciones endocrinológicas constituyen parte importante de la consulta pediátrica, la más frecuente es el hipotiroidismo congénito, grave problema de salud pública que requiere de diagnóstico neonatal. Los avances en el estudio molecular han permitido discernir l... View more
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