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2007 | 1 |
2008 | 1 |
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Detection and validation of copy number variation in X-linked mental retardation.
Cytogenet Genome Res. 2008;123(1-4):44-53. doi: 10.1159/000184691. Epub 2009 Mar 11.
Cytogenet Genome Res. 2008.
PMID: 19287138
Review.
Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disability.
Vanmarsenille L, Verbeeck J, Belet S, Roebroek AJ, Van de Putte T, Nevelsteen J, Callaerts-Vegh Z, D'Hooge R, Marynen P, Froyen G.
Vanmarsenille L, et al. Among authors: nevelsteen j.
PLoS One. 2013 May 13;8(5):e64144. doi: 10.1371/journal.pone.0064144. Print 2013.
PLoS One. 2013.
PMID: 23675524
Free PMC article.
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Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans.
Wu Y, Arai AC, Rumbaugh G, Srivastava AK, Turner G, Hayashi T, Suzuki E, Jiang Y, Zhang L, Rodriguez J, Boyle J, Tarpey P, Raymond FL, Nevelsteen J, Froyen G, Stratton M, Futreal A, Gecz J, Stevenson R, Schwartz CE, Valle D, Huganir RL, Wang T.
Wu Y, et al. Among authors: nevelsteen j.
Proc Natl Acad Sci U S A. 2007 Nov 13;104(46):18163-8. doi: 10.1073/pnas.0708699104. Epub 2007 Nov 7.
Proc Natl Acad Sci U S A. 2007.
PMID: 17989220
Free PMC article.
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