Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome

Autor: Jiraanont, P., Hagerman, R.J., Neri, G., Zollino, M., Murdolo, M., Tassone, F.
Zdroj: In European Journal of Medical Genetics September 2016 59(9):459-462
Databáze: ScienceDirect