يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"MeijersHeijboer, H"', وقت الاستعلام: 0.32s تنقيح النتائج
  1. 1
    Book
    Genetic Predisposition to Gynecologic Cancers

    المؤلفون: MEIJERSHEIJBOER, H

    المصدر: When to Screen in Obstetrics and Gynecology ; page 574-590 ; ISBN 9781416003007

    الاتاحة: http://dx.doi.org/10.1016/b978-1-4160-0300-7.50052-1

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  2. 2
    Academic Journal
    A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

    المؤلفون: Peelen, T, vanVliet, M, PetrijBosch, A, Mieremet, R, Szabo, C, van den Ouweland, AMW, Hogervorst, F, Brohet, R, Ligtenberg, MJL, Teugels, E, vanderLuijt, R, van der Hout, AH, Gille, JJP, Pals, G, Jedema, I, Olmer, R, van Leeuwen, I, Newman, B, Plandsoen, M, vanderEst, M, Brink, G, Hageman, S, Arts, PJW, Bakker, MM, Willems, HW, vanderLooij, E, Neyns, B, Bonduelle, M, Jansen, R, Oosterwijk, JC, Sijmons, R, Smeets, HJM, van Asperen, CJ, MeijersHeijboer, H, Klijn, JGM, deGreve, J, King, MC, Menko, FH, Brunner, HG, Halley, D, vanOmmen, GJB, Vasen, HFA, Cornelisse, CJ, vantVeer, LJ, deKnijff, P, Bakker, E, Devilee, P

    المصدر: Peelen , T , vanVliet , M , PetrijBosch , A , Mieremet , R , Szabo , C , van den Ouweland , AMW , Hogervorst , F , Brohet , R , Ligtenberg , MJL , Teugels , E , vanderLuijt , R , van der Hout , AH , Gille , JJP , Pals , G , Jedema , I , Olmer , R , van Leeuwen , I , Newman , B , Plandsoen , M , vanderEst , M , Brink , G , Hageman , S , Arts , PJW , Bakker , ....

    مصطلحات موضوعية: PROTEIN TRUNCATION TEST, SUSCEPTIBILITY GENE, GERMLINE MUTATIONS, RAPID DETECTION, DNA, FREQUENCY, CARRIERS, 185DELAG, LINKAGE

    الاتاحة: https://hdl.handle.net/11370/301056a5-e7e1-4835-9e18-2d6ecc90b670
    https://research.rug.nl/en/publications/301056a5-e7e1-4835-9e18-2d6ecc90b670

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  3. 3
    A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

    المؤلفون: Peelen, T., Vanvliet, M., Petrijbosch, A., Mieremet, R., Szabo, C., Vandenouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., Vanderluijt, R., Vanderhout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., Vanleeuwen, I., Newman, B., Plandsoen, M., Vanderest, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., Vanderlooij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., Vanasperen, C. J., Meijersheijboer, H., Klijn, J. G. M., Degreve, J., King, M. C., Menko, F. H., Brunner, H. G., Halley, D., Vanommen, G. J. B., Vasen, H. F. A., Cornelisse, C. J., Vantveer, L. J., Peter de Knijff, Bakker, E., Devilee, P.

    المساهمون: Clinical Genetics, Pathology, Medical Oncology, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON), Other departments

    المصدر: American Journal of Human Genetics, 60, 5, pp. 1041-1049
    American Journal of Human Genetics, 60, 1041-1049
    ResearcherID
    American Journal of Human Genetics, 60, 1041-1049. Cell Press
    American Journal of Human Genetics, 60(5), 1041-1049. CELL PRESS
    Scopus-Elsevier
    American journal of human genetics, 60(5), 1041-1049. Cell Press

    مصطلحات موضوعية: RAPID DETECTION, GERMLINE MUTATIONS, DNA, Original Articles, Tumor pathologie, FREQUENCY, CARRIERS, PROTEIN TRUNCATION TEST, SUSCEPTIBILITY GENE, SDG 3 - Good Health and Well-being, LINKAGE, De rol van chromosoomafwijkingen en (anti-)oncogenen in humane tumoren, The role of chromosomal aberrations and (anti-)oncogenes in human tumours, Tumor pathology, 185DELAG, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries)

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::87641196e488ad33abf5c4bfbb9eeac8
    https://hdl.handle.net/2066/25573

    View record in OpenAIRE

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  4. 4
    Periodical
    Spondyloepiphyseal dysplasia, Omani type: Further definition of the phenotypeHow to cite this article: van Roij MHH, Mizumoto S, Yamada S, Morgan T, TanSindhunata MB, MeijersHeijboer H, Verbeke JILM, Markie D, Sugahara K, Robertson SP. 2008. Spondyloepiphyseal dysplasia, Omani type: Further definition of the phenotype. Am J Med Genet Part A 146A:2376–2384.M.H.H. van Roij and S. Mizumoto contributed equally to this work.

    المؤلفون: van Roij, Mirjam H.H., Mizumoto, Shuji, Yamada, Shuhei, Morgan, Tim, TanSindhunata, M.B., MeijersHeijboer, H., Verbeke, J.I.L.M., Markie, David, Sugahara, Kazuyuki, Robertson, Stephen P.

    المصدر: American Journal of Medical Genetics. Part A; September 2008, Vol. 146 Issue: 18 p2376-2384, 9p


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