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Novel genes and mutations in patients affected by recurrent pregnancy loss
(2017-10-10)
Recurrent pregnancy loss is a frequently occurring human infertility-related disease affecting ~1% of women. It has been estimated that the cause remains unexplained in >50% cases which strongly suggests that genetic ...
ASOCIACIÓN DE LA VARIANTE rs11362 DEL GEN DE LA DEFENSINA BETA 1 (DEFB1) CON EL ÍNDICE ICDAS II EN PACIENTES CON CARIES DE LA INFANCIA TEMPRANA
(Biblioteca Digital wdg.biblioUniversidad de Guadalajara, 2020-08-07)
El genotipo homocigoto variante (AA) y alelo variante (A) de la variante rs11362 del gen DEFB1 son factores de riesgo para la Caries de la infancia temprana; no obstante, tenemos que tomar en cuenta que la caries es una ...