Fragile X syndrome: from molecular genetics to therapyHULST, C. D'; KOOY, R. F.Journal of medical genetics. 2009, Vol 46, Num 9, pp 577-584, issn 0022-2593, 8 p.Article

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 et al.Journal of medical genetics. 2004, Vol 41, Num 9, pp 679-683, issn 0022-2593, 5 p.Article

A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11REYNIERS, E; VAN BOGAERT, P; PEETERS, N et al.American journal of human genetics. 1999, Vol 65, Num 5, pp 1406-1412, issn 0002-9297Article

Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13KOOY, R. F; VAN DER VEEN, A. Y; VERLIND, E et al.Human genetics. 1993, Vol 91, Num 5, pp 504-506, issn 0340-6717Article

The Trypanosoma brucei DNA polymerase α core subunit gene is developmentally regulated and linked to a constitutively expressed open reading frameLEEGWATER, P. A. J; STRATING, M; MURPHY, N. B et al.Nucleic acids research. 1991, Vol 19, Num 23, pp 6441-6447, issn 0305-1048Article

Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnosticsROOMS, L; REYNIERS, E; VAN GOETHEM, G et al.Clinical genetics. 2006, Vol 69, Num 1, pp 58-64, issn 0009-9163, 7 p.Article

Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)HOLINSKI-FEDER, E; REYNIERS, E; SCHWAB, S et al.American journal of human genetics. 2000, Vol 66, Num 1, pp 16-25, issn 0002-9297Article

Mean corpuscular hemoglobin is not increased in Fmr1 knockout miceREYNIERS, E; VAN BOCKSTAELE, D. R; DE BOULLE, K et al.Human genetics. 1996, Vol 97, Num 1, pp 49-50, issn 0340-6717Article

Transgenic mouse model for the fragile X syndromeKOOY, R. F; D'HOOGE, R; WILLEMS, P. J et al.American journal of medical genetics. 1996, Vol 64, Num 2, pp 241-245, issn 0148-7299Article

L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsFRANSEN, E; D'HOOGE, R; DE ZEEUW, C. I et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 999-1009, issn 0964-6906Article

Severe mental retardation and macroorchidism without mutation in the FMR1 geneREYNIERS, E; WOLFF, G; TARIVERDIAN, G et al.American journal of medical genetics. 1996, Vol 64, Num 2, pp 408-412, issn 0148-7299Article

Ordering of polymorphic markers in the chromosome region 3p21VAN DEN BERG, A; KOOY, R. F; HULSBEEK, M. M. F et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 225-228, issn 0301-0171Conference Paper

A highly informative dinucleotide repeat polymorphism at D13S201, between RB1 and WNDKOOY, R. F; VERLIND, E; WIJNGAARD, A et al.Human genetics. 1995, Vol 95, Num 5, issn 0340-6717, p. 589Article

Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndromeSTORM, K; HANDIG, I; REYNIERS, E et al.Human genetics. 1998, Vol 102, Num 1, pp 54-56, issn 0340-6717Article

Mildly impaired water maze performance in male Fmr1 knockout miceD'HOOGE, R; NAGELS, G; FRANCK, F et al.Neuroscience. 1997, Vol 76, Num 2, pp 367-376, issn 0306-4522Article

European gene mapping project (EUROGEM) : Breakpoint panels for human chromosomes based on the CEPH reference familiesCOX, S. A; ATTWOOD, J; DIXON, M et al.Annals of human genetics. 1996, Vol 60, pp 447-486, issn 0003-4800, 6Article

Long-term potentiation in the hippocampus of fragile X knockout miceGODFRAIND, J.-M; REYNIERS, E; DE BOULLE, K et al.American journal of medical genetics. 1996, Vol 64, Num 2, pp 246-251, issn 0148-7299Article

On the DNA content of Trypanosoma cruziKOOY, R. F; ASHALL, F; VAN DER PLOEG, M et al.Molecular and biochemical parasitology. 1989, Vol 36, Num 1, pp 73-76, issn 0166-6851Article

Postmortem examination of two fragile X brothers with an FMR1 full mutationREYNIERS, E; MARTIN, J.-J; CRAS, P et al.American journal of medical genetics. 1999, Vol 84, Num 3, pp 245-249, issn 0148-7299Article

CAG repeat contraction in the androgen receptor gene in three brothers with mental retardationKOOY, R. F; REYNIERS, E; STORM, K et al.American journal of medical genetics. 1999, Vol 85, Num 3, pp 209-213, issn 0148-7299Article

MRI as a tool to study brain structure in mouse models for mental retardationVERHOYE, M; SIJBERS, J; KOOY, R. F et al.SPIE proceedings series. 1998, Vol 3337, pp 314-320, isbn 0-8194-2782-9Conference Paper

A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemiaHAWTHORN, L; ROBERTS, T; VERLIND, E et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 3, pp 425-430, issn 0888-7543Article

Influence of fever and flurbiprofen on trypanosome growthZWART, D; BRUN, R; DWINGER, R. H et al.Acta tropica. 1990, Vol 47, Num 2, pp 115-123, issn 0001-706XArticle

Evidence for diploidy in metacyclic forms of African trypanosomesKOOY, R. F; HIRUMI, H; MOLOO, S. K et al.Proceedings of the National Academy of Sciences of the United States of America. 1989, Vol 86, Num 14, pp 5469-5472, issn 0027-8424, 4 p.Article