Presence of markers for virulence in the unique short region or repeat region or both of pseudorabies hybrid virusesBERNS, A; VAN DEN OUWELAND, A; QUINT, W et al.Journal of virology. 1985, Vol 53, Num 1, pp 89-93, issn 0022-538XArticle

The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumorVAN DEN OUWELAND, A. M. W; VERDIJK, M; MANNENS, M. M. A. M et al.Human genetics. 1992, Vol 90, Num 1-2, pp 144-146, issn 0340-6717Article

Identification of the L927P and ΔL1260 mutations in the CFTR geneHERMANS, C. J; VEEZE, H. J; DREXHAGE, V. R et al.Human molecular genetics (Print). 1994, Vol 3, Num 7, pp 1199-1200, issn 0964-6906Article

Rapid antibody test for diagnosing fragile X syndrome : a validation of the techniqueWILLEMSEN, R; SMITS, A; MOHKAMSING, S et al.Human genetics. 1997, Vol 99, Num 3, pp 308-311, issn 0340-6717Article

Common C-to-T substitution at position -480 of the hepatic lipase promoter associated with a lowered lipase activity in coronary artery disease patientsJANSEN, H; VERHOEVEN, A. J. M; WEEKS, L et al.Arteriosclerosis, thrombosis, and vascular biology. 1997, Vol 17, Num 11, pp 2837-2842, issn 1079-5642Article

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA I and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCAI/BRCA2 (CIMBA)OSORIO, A; MILNE, R. L; HEALEY, S et al.British journal of cancer. 2009, Vol 101, Num 12, pp 2048-2054, issn 0007-0920, 7 p.Article

Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial riskBREKELMANS, C. T. M; SEYNAEVE, C; OBDEIJN, I. M et al.Journal of clinical oncology. 2001, Vol 19, Num 4, pp 924-930, issn 0732-183XArticle

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13TAKAHASHI, M; RAPLEY, E; EVANS, D. G et al.Human genetics. 2000, Vol 106, Num 1, pp 58-65, issn 0340-6717Article

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene productsVAN SLEGTENHORST, M; NELLIST, M; NAGELKERKEN, B et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 1053-1057, issn 0964-6906Article

Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndromeHORSTHEMKE, B; MAAT-KIEVIT, A; SLEEGERS, E et al.Journal of medical genetics. 1996, Vol 33, Num 10, pp 848-851, issn 0022-2593Article

DNA testing for fragile X syndrome : implications for parents and familyVAN RIJN, M. A; DE VRIES, B. B. A; TIBBEN, A et al.Journal of medical genetics. 1997, Vol 34, Num 11, pp 907-911, issn 0022-2593Article

The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28 % of the cellsDE GRAAFF, E; DE VRIES, B. B. A; WILLEMSEN, R et al.American journal of medical genetics. 1996, Vol 64, Num 2, pp 302-308, issn 0148-7299Article

Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelTRAUPE, H; VAN DEN OUWELAND, A. M. W; VAN OOST, B. A et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 2, pp 481-483, issn 0888-7543Article

Nucleotide sequence of the DNA region immediately upstream of the human c-sis proto-oncogeneVAN DEN OUWELAND, A. M. W; VAN GRONINGEN, J. J. M; HENDRIKSEN, P. J. M et al.Nucleic acids research. 1987, Vol 15, Num 10, issn 0305-1048, 4349Article

Comparative analysis of the human and feline c-sis-proto-oncogenes. Identification of 5' human c-sis coding sequences that are not homologous to the transforming gene of simian sarcoma virusVAN DEN OUWELAND, A. M. W; BREUER, M. L; STEENBERGH, P. H et al.Biochimica et biophysica acta. 1985, Vol 825, Num 2, pp 140-147, issn 0006-3002Article

Uniparental disomy with and without confined placental mosaicism : A model for trisomic zygote rescueLOS, F. J; VAN OPSTAL, D; VAN DEN BERG, C et al.Prenatal diagnosis. 1998, Vol 18, Num 7, pp 659-668, issn 0197-3851Article

Screening with the FMR1 protein test among mentally retarded malesDE VRIES, B. B. A; MOHKAMSING, S; VAN DEN OUWELAND, A. M. W et al.Human genetics. 1998, Vol 103, Num 4, pp 520-522, issn 0340-6717Article

Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeVAN OOST, B. A; SMITS, A. P. T; DREESEN, J. C. F. M et al.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 320-327, issn 0148-7299Article

Structural analysis of a variant clone of Snyder-Theilen feline sarcoma virusVAN GRONINGEN, J. J. M; VAN DEN OUWELAND, A. M. W; WERBEEK, J. S et al.Virus research. 1987, Vol 8, Num 4, pp 349-361, issn 0168-1702Article

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesVAN DEN OUWELAND, A. M. W; DEELEN, W. H; KUNST, C. B et al.Human molecular genetics (Print). 1994, Vol 3, Num 10, pp 1823-1827, issn 0964-6906Article

The structure of the human c-fes/fps proto-oncogeneROEBROEK, A. J. M; SCHALKEN, J. A; VERBEEK, J. S et al.EMBO journal (Print). 1985, Vol 4, Num 11, pp 2897-2903, issn 0261-4189Article

Frequent loss of the AXINI locus but absence of AXINI gene mutations in adenocarcinomas of the gastro-oesophageal junction with nuclear β-catenin expressionKOPPERT, L. B; VAN DER VELDEN, A. W; VAN DE WETERING, M et al.British journal of cancer. 2004, Vol 90, Num 4, pp 892-899, issn 0007-0920, 8 p.Article

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2HULSEBOS, T. J. M; OSKAM, N. T; BIJIEVELD, E. H et al.British journal of cancer. 1999, Vol 81, Num 7, pp 1150-1154, issn 0007-0920Article

Molecular cloning of the feline c-fes proto-oncogene and construction of a chimeric transforming geneVERBEEK, J. S; VAN DEN OUWELAND, A. M. W; SCHALKEN, J. A et al.Gene (Amsterdam). 1985, Vol 35, Num 1-2, pp 33-43, issn 0378-1119Article

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