检索结果 - Hanne Meijers‐Heijboer

Refine Results
  1. 1
    Genomic profiling of CHEK2*1100delC-mutated breast carcinomas

    Genomic profiling of CHEK2*1100delC-mutated breast carcinomas 由 Maarten P.G. Massink, Irsan Kooi, John W.M. Martens, Quinten Waisfisz, Hanne Meijers‐Heijboer

    出版 2015
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    Clinical Characteristics Affect the Impact of an Uninformative DNA Test Result: The Course of Worry and Distress Experienced by Women Who Apply for Genetic Testing for Breast Cancer

    Clinical Characteristics Affect the Impact of an Uninformative DNA Test Result: The Course of Worry and Distress Experienced by Women Who Apply for Genetic Testing for Breast Cance... 由 Sandra van Dijk, Daniëlle R. M. Timmermans, Hanne Meijers-Heijboer, Aad Tibben, Christi J. van Asperen, Wilma Otten

    出版 2006
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era

    Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era 由 Kyra E. Stuurman, Marieke Joosten, Ineke van der Burgt, Mariet W. Elting, Helger G. Yntema, Hanne Meijers‐Heijboer, Tuula Rinne

    出版 2019
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  4. 4
    Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes

    Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes 由 Dora Hammerl, Maarten P.G. Massink, Marcel Smid, Carolien H. M. van Deurzen, Hanne Meijers‐Heijboer, Quinten Waisfisz, Reno Debets, John W.M. Martens

    出版 2019
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    RB1 mutations and second primary malignancies after hereditary retinoblastoma

    RB1 mutations and second primary malignancies after hereditary retinoblastoma 由 Charlotte J. Dommering, Tamara Marees, Annemarie H. van der Hout, Saskia M. Imhof, Hanne Meijers‐Heijboer, Peter J. Ringens, Flora E. van Leeuwen, Annette C. Moll

    出版 2011
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics

    Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics 由 Lotte Kleinendorst, Ozair Abawi, H.J. van der Kamp, Mariëlle Alders, Hanne Meijers‐Heijboer, Elisabeth F. C. van Rossum, Erica L T van den Akker, Mieke M. van Haelst

    出版 2019
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  7. 7
    The 100-plus Study of cognitively healthy centenarians: rationale, design and cohort description

    The 100-plus Study of cognitively healthy centenarians: rationale, design and cohort description 由 Henne Holstege, Nina Beker, Tamara Dijkstra, Karlijn Pieterse, Elizabeth Wemmenhove, Kimja Schouten, Linette Thiessens, Debbie Horsten, Sterre Rechtuijt, Sietske A.M. Sikkes, Frans van Poppel, Hanne Meijers‐Heijboer, Marc Hulsman, Philip Scheltens

    出版 2018
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Biallelic germline mutations of mismatch‐repair genes

    Biallelic germline mutations of mismatch‐repair genes 由 Jan‐Werner Poley, Anja Wagner, Monique M. C. P. Hoogmans, Fred H. Menko, Carli M.J. Tops, Johan M. Kros, Roel E. Reddingius, Hanne Meijers‐Heijboer, Ernst J. Kuipers, Winand N.M. Dinjens

    出版 2007
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  9. 9
    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease

    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease 由 Niccoló Tesi, Sven J. van der Lee, Marc Hulsman, Iris E. Jansen, Najada Stringa, Natasja M. van Schoor, Hanne Meijers‐Heijboer, Martijn Huisman, Philip Scheltens, Marcel J. T. Reinders, Wiesje M. van der Flier, Henne Holstege

    出版 2018
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  10. 10
    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis

    Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis 由 Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas

    出版 2018
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Survival and prognostic factors in BRCA1-associated breast cancer

    Survival and prognostic factors in BRCA1-associated breast cancer 由 Cecile T.M. Brekelmans, Caroline Seynaeve, M. Menke-Pluymers, Hennie T. Brüggenwirth, Madeleine M.A. Tilanus‐Linthorst, C.C.M. Bartels, Mieke Kriege, Albertus N. van Geel, C. Crépin, Jannet Blom, Hanne Meijers-Heijboer, J.G.M. Klijn

    出版 2005
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  12. 12
    Increased prevalence of BRCA1/2 mutations in women with macrotextured breast implants and anaplastic large cell lymphoma of the breast

    Increased prevalence of BRCA1/2 mutations in women with macrotextured breast implants and anaplastic large cell lymphoma of the breast 由 Mintsje de Boer, Michael Hauptmann, Nathalie J. Hijmering, Carel J.M. van Noesel, Hinne A. Rakhorst, Hanne Meijers‐Heijboer, Jan Paul de Boer, René R. W. J. van der Hulst, Daphne de Jong, Flora E. van Leeuwen

    出版 2020
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  13. 13
    Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic

    Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic 由 Bernadette A. M. Heemskerk‐Gerritsen, Cecile T.M. Brekelmans, Marian B. E. Menke‐Pluymers, A.N. van Geel, Madeleine M.A. Tilanus‐Linthorst, Carina C. M. Bartels, Murly Tan, Hanne Meijers‐Heijboer, Jan G.M. Klijn, Caroline Seynaeve

    出版 2007
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  14. 14
    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

    Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. 由 Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    出版 2013
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  15. 15
    Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

    Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region 由 Carl C.T. Ton, Harri Hirvonen, Hiroshi Miwa, Michael M. Weil, Paula Monaghan, Tim Jordan, Veronica van Heyningen, Nicholas D. Hastie, Hanne Meijers‐Heijboer, Matthias Drechsler, Brigitte Royer‐Pokora, Francis S. Collins, Anand Swaroop, Louise C. Strong, Grady F. Saunders

    出版 1991
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  16. 16
    A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression

    A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression 由 Irsan Kooi, Berber M. Mol, Maarten P.G. Massink, Marcus C. de Jong, Pim de Graaf, Paul van der Valk, Hanne Meijers‐Heijboer, Gertjan J.L. Kaspers, Annette C. Moll, Hein te Riele, Jacqueline Cloos, Josephine C. Dorsman

    出版 2016
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  17. 17
    Whole-genome sequencing in health care

    Whole-genome sequencing in health care 由 Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert

    出版 2013
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  18. 18
    Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i>breast cancer families

    Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i>breast cancer families 由 Inge M. M. Lakeman, Florentine Hilbers, Mar Rodríguez‐Girondo, Andrew Lee, Maaike P.G. Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers‐Heijboer, Jan C. Oosterwijk, Nicoline Hoogerbrugge, Edith Oláh, Hans F. A. Vasen, Christi J. van Asperen, Peter Devilee

    出版 2019
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  19. 19
    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer 由 Andrea E. van der Meulen–de Jong, Marjo van Puijenbroek, Yvonne Hendriks, Carli Tops, Juul Wijnen, Margreet G.E.M. Ausems, Hanne Meijers‐Heijboer, Anja Wagner, Theo A.M. van Os, Annette Bröcker‐Vriends, Hans F. A. Vasen, Hans Morreau

    出版 2004
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  20. 20
    Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence

    Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence 由 Maria B. Tan-Sindhunata, Inge B. Mathijssen, Margriet Smit, Frank Baas, Johanna I. de Vries, J. Patrick van der Voorn, Irma Kluijt, Marleen A. Hagen, Eveline W Blom, Erik A. Sistermans, Hanne Meijers‐Heijboer, Quinten Waisfisz, Marjan M. Weiss, Alexander J. Groffen

    出版 2014
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: