Marynen P - Search Results

1

NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation.

Jun L, Frints S, Duhamel H, Herold A, Abad-Rodrigues J, Dotti C, Izaurralde E, Marynen P, Froyen G. Jun L, et al. Among authors: marynen p. Curr Biol. 2001 Sep 18;11(18):1381-91. doi: 10.1016/s0960-9822(01)00419-5. Curr Biol. 2001. PMID: 11566096 Free article.

2

Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene.

Frints SG, Jun L, Fryns JP, Devriendt K, Teulingkx R, Van den Berghe L, De Vos B, Borghgraef M, Chelly J, Des Portes V, Van Bokhoven H, Hamel B, Ropers HH, Kalscheuer V, Raynaud M, Moraine C, Marynen P, Froyen G. Frints SG, et al. Among authors: marynen p. Am J Med Genet A. 2003 Jun 15;119A(3):367-74. doi: 10.1002/ajmg.a.20195. Am J Med Genet A. 2003. PMID: 12784308

3

X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms.

Frints SG, Froyen G, Marynen P, Fryns JP. Frints SG, et al. Among authors: marynen p. Clin Genet. 2002 Dec;62(6):423-32. doi: 10.1034/j.1399-0004.2002.620601.x. Clin Genet. 2002. PMID: 12485186 Review.

4

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.

Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR, Devriendt K, Fryns JP, Marynen P. Froyen G, et al. Among authors: marynen p. Hum Mutat. 2007 Oct;28(10):1034-42. doi: 10.1002/humu.20564. Hum Mutat. 2007. PMID: 17546640

5

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: marynen p. PLoS One. 2013 May 13;8(5):e64144. doi: 10.1371/journal.pone.0064144. Print 2013. PLoS One. 2013. PMID: 23675524 Free PMC article.

6

X chromosome array-CGH for the identification of novel X-linked mental retardation genes.

Bauters M, Van Esch H, Marynen P, Froyen G. Bauters M, et al. Among authors: marynen p. Eur J Med Genet. 2005 Jul-Sep;48(3):263-75. doi: 10.1016/j.ejmg.2005.04.008. Eur J Med Genet. 2005. PMID: 16179222

7

Clinical study and haplotype analysis in two brothers with Partington syndrome.

Frints SG, Borghgraef M, Froyen G, Marynen P, Fryns JP. Frints SG, et al. Among authors: marynen p. Am J Med Genet. 2002 Nov 1;112(4):361-8. doi: 10.1002/ajmg.10630. Am J Med Genet. 2002. PMID: 12376938

8

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.

Frints SG, Marynen P, Hartmann D, Fryns JP, Steyaert J, Schachner M, Rolf B, Craessaerts K, Snellinx A, Hollanders K, D'Hooge R, De Deyn PP, Froyen G. Frints SG, et al. Among authors: marynen p. Hum Mol Genet. 2003 Jul 1;12(13):1463-74. doi: 10.1093/hmg/ddg165. Hum Mol Genet. 2003. PMID: 12812975

9

Detection and validation of copy number variation in X-linked mental retardation.

Bauters M, Weuts A, Vandewalle J, Nevelsteen J, Marynen P, Van Esch H, Froyen G. Bauters M, et al. Among authors: marynen p. Cytogenet Genome Res. 2008;123(1-4):44-53. doi: 10.1159/000184691. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287138 Review.

10

X-linked mental retardation and epigenetics.

Froyen G, Bauters M, Voet T, Marynen P. Froyen G, et al. Among authors: marynen p. J Cell Mol Med. 2006 Oct-Dec;10(4):808-25. doi: 10.1111/j.1582-4934.2006.tb00526.x. J Cell Mol Med. 2006. PMID: 17125586 Free PMC article. Review.

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