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Number of items: 2.

Vulto-van Silfhout, Anneke T; Rajamanickam, Shivakumar; Jensik, Philip J; Vergult, Sarah; de Rocker, Nina; Newhall, Kathryn J; Raghavan, Ramya; Reardon, Sara N; Jarrett, Kelsey; McIntyre, Tara; Bulinski, Joseph; Ownby, Stacy L; Huggenvik, Jodi I; McKnight, G Stanley; Rose, Gregory M; Cai, Xiang; Willaert, Andy; Zweier, Christiane; Endele, Sabine; de Ligt, Joep; van Bon, Bregje W M; Lugtenberg, Dorien; de Vries, Petra F; Veltman, Joris A; van Bokhoven, Hans; Brunner, Han G; Rauch, Anita; de Brouwer, Arjan P M; Carvill, Gemma L; Hoischen, Alexander; Mefford, Heather C; Eichler, Evan E; Vissers, Lisenka E L M; Menten, Björn; Collard, Michael W; de Vries, Bert B A (2014). Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems. American Journal of Human Genetics, 94(5):649-661.

Collin, Rob W J; Nikopoulos, Konstantinos; Dona, Margo; Gilissen, Christian; Hoischen, Alexander; Boonstra, F Nienke; Poulter, James A; Kondo, Hiroyuki; Berger, Wolfgang; Toomes, Carmel; Tahira, Tomoko; Mohn, Lucas R; Blokland, Ellen A; Hetterschijt, Lisette; Ali, Manir; Groothuismink, Johanne M; Duijkers, Lonneke; Inglehearn, Chris F; Sollfrank, Lea; Strom, Tim M; Uchio, Eiichi; van Nouhuys, C Erik; Kremer, Hannie; Veltman, Joris A; van Wijk, Erwin; Cremers, Frans P M (2013). ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature. Proceedings of the National Academy of Sciences of the United States of America, 110(24):9856-9861.

This list was generated on Sat Jul 20 01:14:21 2019 CEST.