Estadísticas

	Visualizaciones
Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease	42

Seleccione un intervalo de tiempo:

	Visualizaciones
Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease	24

Repositorio digital RUNA