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 |
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Zdroj: | Genome Medicine. 11/27/2017, Vol. 9, p1-16. 16p. 1 Diagram, 2 Charts, 4 Graphs. |
Databáze: | Academic Search Ultimate |
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