Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype
Lamers, Ideke J.C., Reijnders, Margot R.F., Venselaar, Hanka, Kraus, Alison, Jansen, Sandra, de Vries, Bert B.A., Houge, Gunnar, Gradek, Gyri Aasland, Seo, Jieun, Choi, Murim, Chae, Jong-Hee, van der Burgt, Ineke, Pfundt, Rolph, Letteboer, Stef J.F., van Beersum, Sylvia E.C., Dusseljee, Simone, Brunner, Han G., Doherty, Dan, Kleefstra, Tjitske, Roepman, Ronald
Published in American journal of human genetics (02.11.2017)
Published in American journal of human genetics (02.11.2017)
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Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability
Johansson, Stefan, Berland, Siren, Gradek, Gyri Aasland, Bongers, Ernie, de Leeuw, Nicole, Pfundt, Rolph, Fannemel, Madeleine, Rødningen, Olaug, Brendehaug, Atle, Haukanes, Bjørn Ivar, Hovland, Randi, Helland, Gunnar, Houge, Gunnar
Published in American journal of medical genetics. Part A (01.07.2014)
Published in American journal of medical genetics. Part A (01.07.2014)
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Registration of Down syndrome in the Medical Birth Registry of Norway: Validity and time trends
Melve, Kari Klungsøyr, Lie, Rolv Terje, Skjaerven, Rolv, Van Der Hagen, Carl Birger, Gradek, Gyri Aasland, Jonsrud, Christopher, Braathen, Geir J., Irgens, Lorentz M.
Published in Acta obstetricia et gynecologica Scandinavica (01.01.2008)
Published in Acta obstetricia et gynecologica Scandinavica (01.01.2008)
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