Importance of molecular genetic analysis in the diagnosis and classification of congenital hypothyroidism

Targovnik, Hector Manuel

Artículos de revistas

Fecha

2014-03

Registro en:

Targovnik, Hector Manuel; Importance of molecular genetic analysis in the diagnosis and classification of congenital hypothyroidism; Springer; Endrocrine; 45; 2; 3-2014; 163-164

1355-008X

http://hdl.handle.net/11336/18610

1559-0100

CONICET Digital

CONICET

http://repositorioslatinoamericanos.uchile.cl/handle/2250/1850738

Autor

Targovnik, Hector Manuel

Institución

Consejo Nacional de Investigaciones Científicas y Tecnológicas (Argentina)

Resumen

Congenital hypothyroidism (CH) is the most frequent endocrine disease in infants, with the prevalence ratio in the range of 1:2,000–1:4,000 newborns.

Materias

Congenital hypothyroidism

Thyroglobulin genes

Mutation

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