Bleeding in carriers of hemophilia by Plug, Iris, Mauser-Bunschoten, Eveline P., Bröcker-Vriends, Annette H.J.T., van Amstel, Hans Kristian Ploos, van der Bom, Johanna G., van Diemen-Homan, Joanna E.M., Willemse, José, Rosendaal, Frits R.

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Prognostic factors for hereditary cancer distress six months after BRCA1/2 or HNPCC genetic susceptibility testing by van Oostrom, Iris, Meijers-Heijboer, Hanne, Duivenvoorden, Hugo J, Bröcker-Vriends, Annette H.J.T, van Asperen, Christi J, Sijmons, Rolf H, Seynaeve, Caroline, Van Gool, Arthur R, Klijn, Jan G.M, Tibben, Aad

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Comparison of individuals opting for BRCA1/2 or HNPCC genetic susceptibility testing with regard to coping, illness perceptions, illness experiences, family system characteristics... by van Oostrom, Iris, Meijers-Heijboer, Hanne, Duivenvoorden, Hugo J, Bröcker-Vriends, Annette H.J.T, van Asperen, Christi J, Sijmons, Rolf H, Seynaeve, Caroline, Van Gool, Arthur R, Klijn, Jan G.M, Tibben, Aad

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Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians by Hendriks, Yvonne M.C, de Jong, Andrea E, Morreau, Hans, Tops, Carli M.J, Vasen, Hans F, Wijnen, Juul Th, Breuning, Martijn H, Brocker-Vriends, Annette H.J.T

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Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer by DE JONG, Andrea E, VAN PUIJENBROEK, Marjo, VASEN, Hans F. A, MORREAU, Hans, HENDRIKS, Yvonne, TOPS, Carli, WIJNEN, Juul, AUSEMS, Margreet G. E. M, MEIJERS-HEIJBOER, Hanne, WAGNER, Anja, VAN OS, Theo A. M, BRÖCKER-VRIENDS, Annette H. J. T

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients by de Leeuw, Wiljo J. F., Dierssen, JanWillem, Vasen, Hans F. A., Wijnen, Juul Th, Kenter, Gemma G., Meijers-Heijboer, Hanne, Brocker-Vriends, Annette, Stormorken, Astrid, Moller, Pal, Menko, Fred, Cornelisse, Cees J., Morreau, Hans

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A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships by Oostrom, Iris van, Meijers-Heijboer, Hanne, Duivenvoorden, Hugo J., Bröcker-Vriends, Annette H. J. T., van Asperen, Christi J., Sijmons, Rolf H., Seynaeve, Caroline, Van Gool, Arthur R., Klijn, Jan G. M., Riedijk, Samantha R., van Dooren, Silvia, Tibben, Aad

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The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study by van Oostrom, Iris, Meijers-Heijboer, Hanne, Duivenvoorden, Hugo J., Bröcker-Vriends, Annette H. J. T., van Asperen, Christi J., Sijmons, Rolf H., Seynaeve, Caroline, Van Gool, Arthur R., Klijn, Jan G. M., Tibben, Aad

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Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene by Taschner, Peter E.M., Jansen, Jeroen C., Baysal, Bora E., Bosch, Anne, Rosenberg, Efraim H., Bröcker-Vriends, Annette H.J.T., van der Mey, Andel G.L., van Ommen, Gert-Jan B., Cornelisse, Cees J., Devilee, Peter

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A near false-negative finding of mosaic trisomy 21-a cautionary tale by Beverstock, G. C., Hansson, Kerstin, Helderman-Van Den Enden, Apollonia T. J. M., Bröcker-Vriends, Annette, Klumper, F., Bartelings, Margot, Dobbe-Van Meerendonk, Willemijn, Roosmalen, J. V., Kolkman, P. H., Kanhai, H. H. H.

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Somatic origin of inherited haemophilia A by BRÖCKER-VRIENDS, A. H. J. T, BRIËT, E, DREESEN, J. C. F. M, BAKKER, B, REITSMA, P, PANNEKOEK, H, VAN DE KAMP, J. J. P, PEARSON, P. L

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Bleeding in carriers of hemophilia. Commentary by ALEDORT, Louis M, PLUG, Iris, MAUSER-BUNSCHOTEN, Eveline P, BRÖCKER-VRIENDS, Annette H. J. T, KRISTIAN PLOOS VAN AMSTEL, Hans, VAN DER BOM, Johanna G, VAN DIEMEN-HOMAN, Joanna E. M, WILLEMSE, José, ROSENDAAL, Frits R

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