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cancer mutation family phaeochromocytoma breast paraganglioma patient linkage breast cancer tumours immunohistochemistry sdhb immunohistochemistry analysis result chromosome score tumor syndrome germline tumour region marker number haplotype brca 1 netherland change study phaeochromocytoma –paraganglioma syndrome series susceptibility sample locus testing disease model tissue analyses allele fferent department germline mutations search genotyped protein speci ficity absence sdhb immunostaining mitochondrial devilee p genet tumour cells –paraganglioma expression antibody genome-wide candidate staining chromosome 9 easton df 9 q 21-22 sdh mutation genome-wide linkage search sdh enzyme activity easton center identi immunohistochemical multipoint university sdhb expression position erasmus mc germline mutation sdhd genes presence 10.1002/ sequence analysis oldenburg speci
4 Most Recent Publications
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SDHA immunohistochemistry detects germline SDHA gene mutations in apparently sporadic paragangliomas and pheochromocytomas
(Article)
Korpershoek, E. Favier, J. Dooren, M.F. van Herder, W.W. de Tissier, F. Plouin, P.F. Nederveen, F.H. van Dinjens, W.N.M. Gimenez-Roqueplo, A.P. Krijger, R.R. de Gaal, J. Burnichon, N. Gessel, B. van Oudijk, L. Badoual, C. Gadessaud, N. Venisse, A. Bayley, J.P. |
2011-09-01
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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
(Article)
Smit, D.L. Mensenkamp, A.R. Hoefsloot, L.H. Moorselaar, R.J.A. van Starink, T.M. Bayley, J.P. Frank, J. Steensel, M.A.M. van Menko, F. Badeloe, S. Breuning, M.H. Simon, M.E.H. Spaendonck, K.Y. van Aalfs, C. Post, J.G. Shanley, S. Krapels, I.P.C. |
2011-01-01
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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
(Article)
Nederveen, F.H. van Gaal, J. Petri, B.J. Komminoth, P. Pacak, K. Hop, W.C.J. Pollard, P.J. Mannelli, M. Bayley, J.P. Perren, A. Niemann, S. Verhofstad, A.A. Favier, J. Bruïne, A.P. de Maher, E.R. Tissier, F. Méatchi, T. Badoual, C. Bertherat, J. Amar, L. Alataki, D. Marck, E. van Ferrau, F. Korpershoek, E. François, J.F. Herder, W.W. de Peeters, M.P.F.V. Linge, A. van Lenders, J.W. Gimenez-Roqueplo, A.P. Krijger, R.R. de Dinjens, W.N.M. Oldenburg, R. Bruyn, E.M. de Sleddens, H.F. Derkx, P. Rivière, J. Dannenberg, H. |
2009-08-01
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Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus
(Article)
Oldenburg, R. Kroeze-Jansema, K.H.G. Vasen, H. Hoogerbrugge, N. Cornelisse, C.J. Meijers-Heijboer, E.J. Devilee, P. Houwing-Duistermaat, J.J. Bayley, J.P. Dambrot, C. Asperen, C.J. van Ouweland, A.M.W. van den Bakker, B. Beers, E.H. van Nederlof, P.M. |
2008-11-01
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