PRRT2-related phenotypes in patients with a 16p11.2 deletion
Vlaskamp, Danique R.M., Callenbach, Petra M.C., Rump, Patrick, Giannini, Lucia A.A., Brilstra, Eva H., Dijkhuizen, Trijnie, Vos, Yvonne J., van der Kevie-Kersemaekers, Anne-Marie F., Knijnenburg, JeroМова:
english
Журнал:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2018.08.002
Date:
August, 2018
Файл:
PDF, 666 KB
english, 2018