Truncating de novo mutations in the Krüppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphisms.
| Autor: | Stevens, Servi J. C.1 servi.stevens@mumc.nl, van Essen, Anthonie J.2, van Ravenswaaij, Conny M. A.2, Elias, Abdallah F.3, Haven, Jaclyn A.3, Lelieveld, Stefan H.4, Pfundt, Rolph4, Nillesen, Willy M.4, Yntema, Helger G.4, van Roozendaal, Kees1,4, Stegmann, Alexander P.1, Gilissen, Christian4, Brunner, Han G.1,4 |
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| Zdroj: | Genome Medicine. 12/13/2016, Vol. 8, p1-10. 10p. |
| Databáze: | Academic Search Ultimate |
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