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Genetic modifiers in mice: the example of the fragile X mouse model.
Cytogenet Genome Res. 2004;105(2-4):448-54. doi: 10.1159/000078218.
Cytogenet Genome Res. 2004.
PMID: 15237233
Review.
FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis.
Errijgers V, Van Dam D, Gantois I, Van Ginneken CJ, Grossman AW, D'Hooge R, De Deyn PP, Kooy RF.
Errijgers V, et al.
Genes Brain Behav. 2007 Aug;6(6):552-7. doi: 10.1111/j.1601-183X.2006.00282.x. Epub 2006 Nov 3.
Genes Brain Behav. 2007.
PMID: 17083330
Free article.
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Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
Winnepenninckx B, Errijgers V, Hayez-Delatte F, Reyniers E, Frank Kooy R.
Winnepenninckx B, et al. Among authors: errijgers v.
Hum Mutat. 2002 Oct;20(4):249-52. doi: 10.1002/humu.10130.
Hum Mutat. 2002.
PMID: 12325019
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Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).
Van Dam D, Errijgers V, Kooy RF, Willemsen R, Mientjes E, Oostra BA, De Deyn PP.
Van Dam D, et al. Among authors: errijgers v.
Behav Brain Res. 2005 Jul 30;162(2):233-9. doi: 10.1016/j.bbr.2005.03.007.
Behav Brain Res. 2005.
PMID: 15876460
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A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9).
Ramser J, Winnepenninckx B, Lenski C, Errijgers V, Platzer M, Schwartz CE, Meindl A, Kooy RF.
Ramser J, et al. Among authors: errijgers v.
J Med Genet. 2004 Sep;41(9):679-83. doi: 10.1136/jmg.2004.019000.
J Med Genet. 2004.
PMID: 15342698
Free PMC article.
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Effect of genetic background on acoustic startle response in fragile X knockout mice.
Errijgers V, Fransen E, D'Hooge R, De Deyn PP, Kooy RF.
Errijgers V, et al.
Genet Res (Camb). 2008 Aug;90(4):341-5. doi: 10.1017/S0016672308009415.
Genet Res (Camb). 2008.
PMID: 18840308
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Family MRX9 revisited: further evidence for locus heterogeneity in MRX.
Winnepenninckx B, Errijgers V, Reyniers E, De Deyn PP, Abidi FE, Schwartz CE, Kooy RF.
Winnepenninckx B, et al. Among authors: errijgers v.
Am J Med Genet. 2002 Sep 15;112(1):17-22. doi: 10.1002/ajmg.10663.
Am J Med Genet. 2002.
PMID: 12239714
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