检索结果 - Devilee, Peter

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

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

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Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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