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deletion chromosome osteochondroma desmoid patient region tumours analysis tumor ext 1 ext 1 gene cartilage cap mutation study array genet clone nonhereditary osteochondromas genomic tumour trisomy 17 mosaicism probe trisomy nonhereditary sample result cancer expression fap-associated array-cgh mosaicism cartilage table center tissue ratio chromosome 8 q netherland array cgh trisomy 17 desmoid tumours epilepsy allele segment mlpa analysis leiden university chromosome 8 phenotypic effect growth university leiden hybridization apc gene number origin frequency figure abnormality suppressor genomic hybridization phenotype phenotypic reference plate non-fap szuhai k desmoid tumors tumor suppressor gene nuclei seizure article perichondrium germline sa paulo ctnnb department ext 2 genes 8 q 24 component 6 p 21.2-p
5 Most Recent Publications
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Another rare prenatal case of post-zygotic mosaic trisomy 17
(Article)
Vries, F.A. de Govaerts, L.C. Knijnenburg, J. Knapen, M.F.C.M. Oudesluijs, G.G. Lont, D. Noomen, P. Graaff, K. Srebniak, M. Opstal, D. van |
2013-03-22
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Familial adenomatous polyposis-associated desmoids display significantly more genetic changes than sporadic desmoids
(Article)
Robanus-Maandag, E.C. Bosch, C.A.J. Alman, B.A. Tejpar, S. Devilee, P. Fodde, R. Amini-Nik, S. Knijnenburg, J. Szuhai, K. Cervera, P. Poon, R. Eccles, D. Radice, P. Giovannini, M. |
2011-09-09
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Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy
(Article)
Krepischi, A.C.V. Knijnenburg, J. Bertola, D.R. Kim, C.A. Pearson, P.L. Bijlsma, E. Szuhai, K. Kok, F. Vianna-Morgante, A.M. Rosenberg, C. |
2010-12-01
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Interstitial deletion of 6q without phenotypic effect
(Article)
Hansson, K.B. Szuhai, K. Knijnenburg, J. Haeringen, A. van Pater, J. de |
2007-06-15
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The role of EXT1 in nonhereditary osteochondroma: Identification of homozygous deletions
(Article)
Hameetman, L. Szuhai, K. Yavas, A. Knijnenburg, J. Duin, M. van Dekken, H. van Taminiau, A.H.M. Cleton-Jansen, A. Bovée, J.V.M.G. Hogendoorn, P.C.W. |
2007-03-07
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