Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair
Bauters, Marijke, Van Esch, Hilde, Friez, Michael J, Boespflug-Tanguy, Odile, Zenker, Martin, Vianna-Morgante, Angela M, Rosenberg, Carla, Ignatius, Jaakko, Raynaud, Martine, Hollanders, Karen, Govaerts, Karen, Vandenreijt, Kris, Niel, Florence, Blanc, Pierre, Stevenson, Roger E, Fryns, Jean-Pierre, Marynen, Peter, Schwartz, Charles E, Froyen, Guy
Published in Genome Research (01.06.2008)
Published in Genome Research (01.06.2008)
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Dosage-Dependent Severity of the Phenotype in Patients with Mental Retardation Due to a Recurrent Copy-Number Gain at Xq28 Mediated by an Unusual Recombination
Vandewalle, Joke, Van Esch, Hilde, Govaerts, Karen, Verbeeck, Jelle, Zweier, Christiane, Madrigal, Irene, Mila, Montserrat, Pijkels, Elly, Fernandez, Isabel, Kohlhase, Jürgen, Spaich, Christiane, Rauch, Anita, Fryns, Jean-Pierre, Marynen, Peter, Froyen, Guy
Published in American journal of human genetics (11.12.2009)
Published in American journal of human genetics (11.12.2009)
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Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
Froyen, Guy, Corbett, Mark, Vandewalle, Joke, Jarvela, Irma, Lawrence, Owen, Meldrum, Cliff, Bauters, Marijke, Govaerts, Karen, Vandeleur, Lucianne, Van Esch, Hilde, Chelly, Jamel, Sanlaville, Damien, van Bokhoven, Hans, Ropers, Hans-Hilger, Laumonnier, Frederic, Ranieri, Enzo, Schwartz, Charles E., Abidi, Fatima, Tarpey, Patrick S., Futreal, P. Andrew, Whibley, Annabel, Raymond, F. Lucy, Stratton, Michael R., Fryns, Jean-Pierre, Scott, Rodney, Peippo, Maarit, Sipponen, Marjatta, Partington, Michael, Mowat, David, Field, Michael, Hackett, Anna, Marynen, Peter, Turner, Gillian, Gécz, Jozef
Published in American journal of human genetics (01.02.2008)
Published in American journal of human genetics (01.02.2008)
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Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
FROYEN, Guy, BAUTERS, Marijke, MARYNEN, Peter, GECZ, Jozef, TURNER, Gillian, BOYLE, Jackie, VAN ESCH, Hilde, GOVAERTS, Karen, VAN BOKHOVEN, Hans, ROPERS, Hans-Hilger, MORAINE, Claude, CHELLY, Jamel, FRYNS, Jean-Pierre
Published in Human genetics (01.06.2007)
Published in Human genetics (01.06.2007)
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Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
Froyen, Guy, Corbett, Mark, Vandewalle, Joke, Jarvela, Irma, Lawrence, Owen, Meldrum, Cliff, Bauters, Marijke, Govaerts, Karen, Vandeleur, Lucianne, Esch, Hilde Van, Chelly, Jamel, Saniaville, Damien, Bokhoven, Hans van, Ropers, Hans- Hilger, Laumonnier, Frederic, Ranieri, Enzo, Schwartz, Charles E, Abidi, Fatima, Tarpey, Patrick S, Futreal, P Andrew, Whibley, Annabel, Raymond, F Lucy, Stratton, Michael R, Fryns, Jean-Pierre, Scott, Rodney, Peippo, Maarit, Sipponen, Marjatta, Partington, Michael, Mowat, David, Field, Michael, Hackett, Anna, Marynen, Peter, Turner, Gillian, Gécz, Jozef
Published in American journal of human genetics (08.02.2008)
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Published in American journal of human genetics (08.02.2008)
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Structural analysis of a nanoparticle containing a lipid bilayer used for detergent-free extraction of membrane proteins
Jamshad, Mohammed, Grimard, Vinciane, Idini, Ilaria, Knowles, Tim J., Dowle, Miriam R., Schofield, Naomi, Sridhar, Pooja, Lin, Yupin, Finka, Rachael, Wheatley, Mark, Thomas, Owen R. T., Palmer, Richard E., Overduin, Michael, Govaerts, Cédric, Ruysschaert, Jean-Marie, Edler, Karen J., Dafforn, Tim R.
Published in Nano research (01.03.2015)
Published in Nano research (01.03.2015)
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