Artículos de revistas
Importance of molecular genetic analysis in the diagnosis and classification of congenital hypothyroidism
Fecha
2014-03Registro 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
1559-0100
CONICET Digital
CONICET
Autor
Targovnik, Hector Manuel
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.