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Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2
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Published in Journal of clinical oncology (01.11.1999)
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Yield of Lynch Syndrome Surveillance for Patients With Pathogenic Variants in DNA Mismatch Repair Genes
Goverde, A, Eikenboom, E.L, Viskil, E.L, Bruno, M.J, Doukas, M, Dinjens, W.N.M, Dubbink, H.J, van den Ouweland, A.M.W, Hofstra, R.M.W, Wagner, A, Spaander, M.C.W
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A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands
van Minkelen, R., van Bever, Y., Kromosoeto, J.N.R., Withagen-Hermans, C.J., Nieuwlaat, A., Halley, D.J.J., van den Ouweland, A.M.W.
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Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes
Lammens, C. R. M., Bleiker, E. M. A., Verhoef, S., Ausems, M. G. E. M., Majoor-Krakauer, D., Sijmons, R. H., Hes, F. J., Gómez-García, E. B., Van Os, T. A. M., Spruijt, L., van der Luijt, R. B., van den Ouweland, A. M. W., Ruijs, M. W. G., Gundy, C., Nagtegaal, T., Aaronson, N. K.
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Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy
Seynaeve, C, Verhoog, L.C, van de Bosch, L.M.C, van Geel, A.N, Menke-Pluymers, M, Meijers-Heijboer, E.J, van den Ouweland, A.M.W, Wagner, A, Creutzberg, C.L, Niermeijer, M.F, Klijn, J.G.M, Brekelmans, C.T.M
Published in European journal of cancer (1990) (01.05.2004)
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Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families
Verhoog, L.C., van den Ouweland, A.M.W., Berns, E., van Veghel-Plandsoen, M.M., van Staveren, I.L., Wagner, A., Bartels, C.C.M., Tilanus-Linthorst, M.M.A., Devilee, P., Seynaeve, C., Halley, D.J.J., Niermeijer, M.F., Klijn, J.G.M., Meijers-Heijboer, H.
Published in European journal of cancer (1990) (01.11.2001)
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The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data
Dohle, G.R., Veeze, H.J., Overbeek, S.E., van den Ouweland, A.M.W., Halley, D.J.J., Weber, R.F.A., Niermeijer, M.F.
Published in Human reproduction (Oxford) (01.02.1999)
Published in Human reproduction (Oxford) (01.02.1999)
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Hyperechogenic fetal bowel: counseling difficulties
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Published in European journal of medical genetics (01.10.2005)
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Geographic distribution within the Netherlands of families with specific mutations in EIRCA1 and BRCA2
Verhoog, L, Meijers-Heijboer, E.J., Wagner, A., Seynaeve, C., van den Ouweland, A.M.W., Halley, D.J.J., Devilee, P., Klijn, J.G.M.
Published in European journal of cancer (1990) (01.09.1998)
Published in European journal of cancer (1990) (01.09.1998)
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Survival in BRCA1-associated breast cancer: long-term follow-up and prognostic factors
Brekelmans, C.T.M, Seynaeve, C, Menke-Pluymers, M, Tilanus-Linthorst, M.M.A, Bartels, C.C.M, Crepin, E, Blom, J, van den Ouweland, A.M.W, Meijers-Heijboer, H, Klijn, J.G.M
Published in European journal of cancer supplements (01.03.2004)
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Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene
Verhoef, S., Vrtel, R., Bakker, L., Stolte-Dijkstra, I., Nellist, M., Begeer, J.H., Zaremba, J., Jozwiak, S., Tempelaars, A.M.P., Lindhout, D., Halley, D.J.J., van den Ouweland, A.M.W.
Published in Human mutation (1998)
Published in Human mutation (1998)
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Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients
Wang, Q, Verhoef, S, Tempelaars, AMP, Bakker, PLG, Vrtel, R, Hesseling-Janssen, ALW, Nellist, M, Oranje, AP, Stroink, H, Lindhout, D, Halley, DJJ, van den Ouweland, AMW
Published in Human mutation (1998)
Published in Human mutation (1998)
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Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region
van den Ouweland, A.M.W., Knoop, M.T., Knoers, V.V.A.M., Markslag, P.W.B., Rocchi, M., Warren, S.T., Ropers, H.H., Fahrenholz, F., Monnens, L.A.H., van Oost, B.A.
Published in Genomics (San Diego, Calif.) (01.08.1992)
Published in Genomics (San Diego, Calif.) (01.08.1992)
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Two polymorphisms at the DXS539 locus
VAN DEN HURK, J. A. J. M, DREESEN, J. C. F. M, VAN DEN BERG, H, VAN BENNEKOM, C. A, VAN DEN OUWELAND, A. M. W, VAN OOST, B. A
Published in Nucleic acids research (11.04.1991)
Published in Nucleic acids research (11.04.1991)
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Large deletion at the TSC1 locus in a family with tuberous sclerosis complex
Nellist, M, Sancak, O, Goedbloed, M A, van Veghel-Plandsoen, M, Maat-Kievit, A, Lindhout, D, Eussen, B H, de Klein, A, Halley, D J J, van den Ouweland, A M W
Published in Genetic testing (01.09.2005)
Published in Genetic testing (01.09.2005)
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DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene
van den Ouweland, A M, de Vries, B B, Bakker, P L, Deelen, W H, de Graaff, E, van Hemel, J O, Oostra, B A, Niermeijer, M F, Halley, D J
Published in American journal of medical genetics (15.07.1994)
Published in American journal of medical genetics (15.07.1994)
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