Long-term survival and transmission of INII-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome von AMMERLAAN, A. C. J, ARAROU, A, HOUBEN, M. P. W. A, BAAS, F, TIJSSEN, C. C, TEEPEN, J. L. J. M, WESSELING, P, HULSEBOS, T. J. M

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SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis von Hulsebos, TJM, Kenter, SB, Jakobs, ME, Baas, F, Chong, B, Delatycki, MB

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A PstI polymorphism associated with CRYBA4 on human chromosome 22 von Bijlsma, E K, Hulsebos, T J

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Molecular-genetic characterisation of gliomas that recur as same grade or higher grade tumours von Hulsebos, T J M, Troost, D, Leenstra, S

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Cloning, Mapping, and Expression Analysis of a Gene Encoding a Novel Mammalian EGF-Related Protein (SCUBE1) von Grimmond, Sean, Larder, Rachel, Van Hateren, Nick, Siggers, Pam, Hulsebos, Theo J.M., Arkell, Ruth, Greenfield, Andy

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Secondary meningioma in a long-term survivor of atypical teratoid/rhabdoid tumour with a germline INI1 mutation von Ammerlaan, A. C. J., Houben, M. P. W. A., Tijssen, C. C., Wesseling, P., Hulsebos, T. J. M.

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GOA, a Novel Gene Encoding a Ring Finger B-Box Coiled-Coil Protein, Is Overexpressed in Astrocytoma von Vandeputte, Dmitri A.A., Meije, Clifton B., van Dartel, Maaike, Leenstra, Sieger, IJlst-Keizers, Helen, Das, Pranab K., Troost, Dirk, Bosch, D.Andries, Baas, Frank, Hulsebos, Theo J.M.

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Genetic sub‐types of human malignant astrocytoma correlate with survival von Leenstra, Sieger, Oskam, Niels T., Bijleveld, Engelien H., Bosch, D. Andries, Troost, Dirk, Hulsebos, Theo J. M.

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Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter–22q11.2 von Hulsebos, T J M, Oskam, N T, Bijleveld, E H, Westerveld, A, Hermsen, M A, Ouweland, A M W van den, Hamel, B C

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Limited contribution of interchromosomal gene conversion to NF1 gene mutation von LUIJTEN, M, FAHSOLD, R, MISCHUNG, C, WESTERVELD, A, NÜRNBERG, P, HULSEBOS, T. J. M

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Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22 von Luijten, M, Redeker, S, Minoshima, S, Shimizu, N, Westerveld, A, Hulsebos, T J

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Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28 von BOLHUIS, P. A, HENSELS, G. W, HULEBOS, T. J. M, BAAS, F, BARTH, P. G

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Molecular analysis of genetic changes in ependymomas von Bijlsma, Emilia K., Voesten, Annet M. J., Bijleveld, Engelien H., Troost, Dirk, Westerveld, Andries, Mérel, Philippe, Thomas, Gilles, Hulsebos, Theo J. M.

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Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22 von Luijten, M, Wang, Y, Smith, B T, Westerveld, A, Smink, L J, Dunham, I, Roe, B A, Hulsebos, T J

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Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas von Luijten, M, Redeker, S, van Noesel, M M, Troost, D, Westerveld, A, Hulsebos, T J

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Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis von Leenstra, S, Bijlsma, E K, Troost, D, Oosting, J, Westerveld, A, Bosch, D A, Hulsebos, T J

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Radiosensitivity and TP 53, EGFR amplification and LOH10 analysis of primary glioma cell cultures von GERLACH, Bärbel, HARDER, Anna H, HULSEBOS, Theo J. M, LEENSTRA, Sieger, SLOTMAN, Berend J, VANDERTOP, W. Peter, HARTMANN, Karl-Axel, SMINIA, Peter

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Analysis of mutations in the SCH gene in schwannomas von Bijlsma, Emilia K., Merel, Philippe, Bosch, D. Andries, Westerveld, Andries, Delattre, Olivier, Thomas, Gilles, Hulsebos, Theo J. M.

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Identification and characterization of NF1-related loci on human chromosomes 22, 14 and 2 von HULSEBOS, T. J. M, BIJILVELD, E. H, RIEGMAN, P. H. J, SMINK, L. J, DUNHAM, I

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Nucleotide sequence of the filamentous bacteriophage M13 DNA genome: comparison with phage fd von van Wezenbeek, Peter M.G.F., Hulsebos, Theo J.M., Schoenmakers, John G.G.

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