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

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11YUAN-QING WU; HEUTINK, P; DE VRIES, B. B. A et al.Human molecular genetics (Print). 1994, Vol 3, Num 1, pp 167-171, issn 0964-6906Article

Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type I syndromeBECKERS, A; ABS, R; REYNIERS, E et al.The Journal of clinical endocrinology and metabolism. 1994, Vol 79, Num 5, pp 1498-1502, issn 0021-972XArticle

Distil myopathy with upper limb predominance caused by filamin C haploinsufficiencyGUERGUELTCHEVA, V; PEETERS, K; YDENS, E et al.Neurology. 2011, Vol 77, Num 24, pp 2105-2114, issn 0028-3878, 10 p.Article

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

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

Gene conversion between red and defective green opsin gene in blue cone monochromacyREYNIERS, E; VAN THIENEN, M.-N; MEIRE, F et al.Genomics (San Diego, Calif.). 1995, Vol 29, Num 2, pp 323-328, issn 0888-7543Article

Alternative splicing in the fragile X gene FMR1VERKERK, A. J. M. H; DE GRAAFF, E; OOSTRA, B. A et al.Human molecular genetics (Print). 1993, Vol 2, Num 4, pp 399-404, issn 0964-6906Article

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

Positional cloning of a gene involved in hereditary multiple exostosesWUYTS, W; VAN HUL, M; BOSSUYT, P et al.Human molecular genetics (Print). 1996, Vol 5, Num 10, pp 1547-1557, issn 0964-6906Article

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

Founder effect in a Belgian-Dutch fragile X populationBUYLE, S; REYNIERS, E; VITS, L et al.Human genetics. 1993, Vol 92, Num 3, pp 269-272, issn 0340-6717Article

Segregation of the fragile X mutation from an affected male to his normal daughterWILLEMS, P. J; VAN ROY, B; DE BOULLE, K et al.Human molecular genetics (Print). 1992, Vol 1, Num 7, pp 511-515, issn 0964-6906Article

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

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome IIWUYTS, W; SARVAN RAMLAKHAN; CONRAD, E. U et al.American journal of human genetics. 1995, Vol 57, Num 2, pp 382-387, issn 0002-9297Article

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAMVITS, L; VAN CAMP, G; WINTER, R. M et al.Nature genetics. 1994, Vol 7, Num 3, pp 408-413, issn 1061-4036Article

An EcoRI RFLP in the 5' region of the human NF1 geneREYNIERS, E; DE BOULLE, K; MARCHUK, D. A et al.Human genetics. 1993, Vol 92, Num 6, issn 0340-6717, p. 631Article