Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.

Autor: Wilfert, Amy B.1,2, Sulovari, Arvis1,2, Turner, Tychele N.1,2, Coe, Bradley P.1, Eichler, Evan E.1,2 eee@gs.washington.edu
Zdroj: Genome Medicine. 11/27/2017, Vol. 9, p1-16. 16p. 1 Diagram, 2 Charts, 4 Graphs.
Databáze: Academic Search Ultimate