Søgeresultater - Devilee, Peter

13(th) General Meeting of The Breast Cancer Linkage Consortium, November 29-December 1, 1999, Amsterdam, The Netherlands af Devilee, Peter

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Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes af Bayley, Jean-Pierre, Devilee, Peter

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The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency af Bayley, Jean-Pierre, Devilee, Peter, Taschner, Peter EM

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Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells af Cervera, Ana M, Bayley, Jean-Pierre, Devilee, Peter, McCreath, Kenneth J

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BRCA1 Mutation Analysis in a Portuguese Population with Early-Onset Breast and/or Ovarian Cancer af Soares, Raquel, van Eijk, Ronald, Dias, Aureliano, Botelho, Mónica, Costa, Carla, Amendoeira, Isabel, Lopes, Carlos, Devilee, Peter, Schmitt, Fernando

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Survey on Physicians' Knowledge and Training Needs in Genetic Counseling in Germany af Dick, Julia, Aue, Viktoria, Wesselmann, Simone, Brédart, Anne, Dolbeault, Sylvie, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita K., Rhiem, Kerstin

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Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis af Hensen, Erik F, Goeman, Jelle J, Oosting, Jan, Van der Mey, Andel GL, Hogendoorn, Pancras CW, Cremers, Cor WRJ, Devilee, Peter, Cornelisse, Cees J

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Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses af van der Klift, Heleen M, Jansen, Anne M L, van der Steenstraten, Niki, Bik, Elsa C, Tops, Carli M J, Devilee, Peter, Wijnen, Juul T

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Correction: Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2 af Mesman, Romy L. S., Calléja, Fabienne M. G. R., de la Hoya, Miguel, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2 af Mesman, Romy L. S., Calléja, Fabienne M. G. R., de la Hoya, Miguel, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Psychosocial problems in women attending French, German and Spanish genetics clinics before and after targeted or multigene testing results: an observational prospective study af Brédart, Anne, Kop, Jean-Luc, Dick, Julia, Cano, Alejandra, De Pauw, Antoine, Anota, Amélie, Brunet, Joan, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita, Dolbeault, Sylvie

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The functional impact of variants of uncertain significance in BRCA2 af Mesman, Romy L. S., Calléja, Fabienne M. G. R., Hendriks, Giel, Morolli, Bruno, Misovic, Branislav, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Information needs on breast cancer genetic and non-genetic risk factors in relatives of women with a BRCA1/2 or PALB2 pathogenic variant af Brédart, Anne, De Pauw, Antoine, Anota, Amélie, Tüchler, Anja, Dick, Julia, Müller, Anita, Kop, Jean-Luc, Rhiem, Kerstin, Schmutzler, Rita, Devilee, Peter, Stoppa-Lyonnet, Dominique, Dolbeault, Sylvie

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Clustering of known low and moderate risk alleles rather than a novel recessive high‐risk gene in non‐BRCA1/2 sib trios affected with breast cancer af Hilbers, Florentine S., van ‘t Hof, Peter J., Meijers, Caro M., Mei, Hailiang, Michailidou, Kyriaki, Dennis, Joe, Hogervorst, Frans B. L., Nederlof, Petra M., van Asperen, Christi J., Devilee, Peter

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Exome Sequencing of Germline DNA from Non-BRCA1/2 Familial Breast Cancer Cases Selected on the Basis of aCGH Tumor Profiling af Hilbers, Florentine S., Meijers, Caro M., Laros, Jeroen F. J., van Galen, Michiel, Hoogerbrugge, Nicoline, Vasen, Hans F. A., Nederlof, Petra M., Wijnen, Juul T., van Asperen, Christi J., Devilee, Peter

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Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma af Bayley, Jean-Pierre, van Minderhout, Ivonne, Hogendoorn, Pancras C. W., Cornelisse, Cees J., van der Wal, Annemieke, Prins, Frans A., Teppema, Luc, Dahan, Albert, Devilee, Peter, Taschner, Peter E. M.

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A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer af Middeldorp, Anneke, Jagmohan-Changur, Shantie, Helmer, Quinta, van der Klift, Heleen M, Tops, Carli MJ, Vasen, Hans FA, Devilee, Peter, Morreau, Hans, Houwing-Duistermaat, Jeanine J, Wijnen, Juul T, van Wezel, Tom

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The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family af Hensen, Erik F, Jansen, Jeroen C, Siemers, Maaike D, Oosterwijk, Jan C, Vriends, Annette HJT, Corssmit, Eleonora PM, Bayley, Jean-Pierre, van der Mey, Andel GL, Cornelisse, Cees J, Devilee, Peter

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Familial Adenomatous Polyposis-Associated Desmoids Display Significantly More Genetic Changes than Sporadic Desmoids af Robanus-Maandag, Els, Bosch, Cathy, Amini-Nik, Saeid, Knijnenburg, Jeroen, Szuhai, Karoly, Cervera, Pascale, Poon, Raymond, Eccles, Diana, Radice, Paolo, Giovannini, Marco, Alman, Benjamin A., Tejpar, Sabine, Devilee, Peter, Fodde, Riccardo

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Genetic clinicians' confidence in BOADICEA comprehensive breast cancer risk estimates and counselees' psychosocial outcomes: A prospective study af Brédart, Anne, De Pauw, Antoine, Tüchler, Anja, Lakeman, Inge M. M., Anota, Amélie, Rhiem, Kerstin, Schmutzler, Rita, van Asperen, Christi J., Devilee, Peter, Stoppa‐Lyonnet, Dominique, Kop, Jean‐Luc, Dolbeault, Sylvie

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