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

Strategy for reliable prenatal detection of normal male carriers of the fragile X syndromeHALLEY, D; VAN DEN OUWELAND, A; DEELEN, W et al.American journal of medical genetics. 1994, Vol 51, Num 4, pp 471-473, issn 0148-7299Article

Rapid antibody test for fragile X syndromeWILLEMSEN, R; MOHKAMSING, S; DE VRIES, B et al.Lancet (British edition). 1995, Vol 345, Num 8958, pp 1147-1148, issn 0140-6736Article

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

Cognitive impairment in tuberous sclerosis complex is a multifactorial conditionJANSEN, F. E; VINCKEN, K. L; VAN HUFFELEN, A. C et al.Neurology. 2008, Vol 70, Num 12, pp 916-923, issn 0028-3878, 8 p.Article

Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells : a new appraisalWILLEMSEN, R; LOS, F; MOHKAMSING, S et al.Journal of medical genetics. 1997, Vol 34, Num 3, pp 250-251, issn 0022-2593Article

The human renin-binding protein gene (RENBP) maps in Xq28VAN DEN OUWELAND, A. M. W; VERDIJK, M; KIOCHIS, P et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 279-281, issn 0888-7543Article

Identification and characterization of a new gene in the human Xq28 regionVAN DEN OUWELAND, A. M. W; KIOSCHIS, P; VERDIJK, M et al.Human molecular genetics (Print). 1992, Vol 1, Num 4, pp 269-273, issn 0964-6906Article

Characterization of the feline c-abl proto-oncogeneSCHALKEN, J. A; VAN DEN OUWELAND, A. M. W; BLOEMERS, H. P. J et al.Biochimica et biophysica acta. 1985, Vol 824, Num 2, pp 104-112, issn 0006-3002Article

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

Overlapping neurologic and cognitive phenotypes in patients with TSC1 or TSC2 mutationsJANSEN, F. E; BRAAMS, O; VAN NIEUWENHUIZEN, O et al.Neurology. 2008, Vol 70, Num 12, pp 908-915, issn 0028-3878, 8 p.Article

Mutational spectrum of the TSC 1 gene in a cohort of 225 tuberous sclerosis complex patients : no evidence for genotype-phenotype correlationVAN SLEGTENHORST, M; VERHOEF, S; VAN DEN OUWELAND, A et al.Journal of medical genetics. 1999, Vol 36, Num 4, pp 285-289, issn 0022-2593Article

Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1VERHOOG, L. C; BREKELMANS, C. T. M; DEVILEE, P et al.Lancet (British edition). 1998, Vol 351, Num 9099, pp 316-321, issn 0140-6736Article

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34VAN SLEGTENHORST, M; DE HOOGT, R; BURLEY, M et al.Science (Washington, D.C.). 1997, Vol 277, Num 5327, pp 805-808, issn 0036-8075Article

Hyperechogenic fetal bowel : counseling difficultiesMARCUS-SOEKARMAN, D; OFFERMANS, J; VAN DEN OUWELAND, A. M. W et al.European journal of medical genetics. 2005, Vol 48, Num 4, pp 421-425, issn 1769-7212, 5 p.Article

The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens : clinical, electrophysiological and genetic dataDOHLE, G. R; VEEZE, H. J; OVERBEEK, S. E et al.Human reproduction (Oxford. Print). 1999, Vol 14, Num 2, pp 371-374, issn 0268-1161Article

Renatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescent in situ hybridization in amniotic fluid cells : a case report of Pallister-Killian syndromeLOS, F. J; VAN OPSTAL, D; SCHOL, M. P et al.Prenatal diagnosis. 1995, Vol 15, Num 12, pp 1155-1159, issn 0197-3851Article

Two polymorphisms at the DXS539 locusVAN DEN HURK, J. A. J. M; DREESEN, J. C. F. M; VAN DEN BERG, H et al.Nucleic acids research. 1991, Vol 19, Num 7, issn 0305-1048, p. 1723Article