Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas
Christiaans, I, Kenter, S B, Brink, H C, van Os, T A M, Baas, F, van den Munckhof, P, Kidd, A M J, Hulsebos, T J M
Published in Journal of medical genetics (01.02.2011)
Published in Journal of medical genetics (01.02.2011)
Get full text
Journal Article
Long-term survival and transmission of INII-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome
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
Published in British journal of cancer (29.01.2008)
Published in British journal of cancer (29.01.2008)
Get full text
Journal Article
SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis
Hulsebos, TJM, Kenter, SB, Jakobs, ME, Baas, F, Chong, B, Delatycki, MB
Published in Clinical genetics (01.01.2010)
Published in Clinical genetics (01.01.2010)
Get full text
Journal Article
Molecular-genetic characterisation of gliomas that recur as same grade or higher grade tumours
Hulsebos, T J M, Troost, D, Leenstra, S
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2004)
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2004)
Get full text
Journal Article
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2
HULSEBOS, T. J. M, OSKAM, N. T, BIJIEVELD, E. H, WESTERVELD, A, HERMSEN, M. A, VAN DEN OUWELAND, A. M. W, HAMEL, B. C, TIJSSEN, C. C
Published in British Journal of Cancer (01.12.1999)
Published in British Journal of Cancer (01.12.1999)
Get full text
Journal Article
Limited contribution of interchromosomal gene conversion to NF1 gene mutation
LUIJTEN, M, FAHSOLD, R, MISCHUNG, C, WESTERVELD, A, NÜRNBERG, P, HULSEBOS, T. J. M
Published in Journal of medical genetics (01.07.2001)
Published in Journal of medical genetics (01.07.2001)
Get full text
Journal Article
Identification and characterization of NF1-related loci on human chromosomes 22, 14 and 2
Hulsebos, T J, Bijleveld, E H, Riegman, P H, Smink, L J, Dunham, I
Published in Human genetics (01.07.1996)
Published in Human genetics (01.07.1996)
Get more information
Journal Article
Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome
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
Published in British journal of cancer (29.01.2008)
Published in British journal of cancer (29.01.2008)
Get full text
Journal Article
New distal marker closely linked to the fragile X locus
Hulsebos, T J, Oostra, B A, Broersen, S, Smits, A, van Oost, B A, Westerveld, A
Published in Human genetics (01.07.1991)
Published in Human genetics (01.07.1991)
Get more information
Journal Article
Limited contribution of interchromosomal gene conversion toNF1 gene mutation
Luijten, M, Fahsold, R, Mischung, C, Westerveld, A, Nürnberg, P, Hulsebos, T J M
Published in Journal of medical genetics (01.07.2001)
Published in Journal of medical genetics (01.07.2001)
Get full text
Journal Article
Identification of the Human βA2 Crystallin Gene ( CRYBA2): Localization of the Gene on Human Chromosome 2 and of the Homologous Gene on Mouse Chromosome 1
Hulsebos, T.J.M., Cerosaletti, K.M., Fournier, R.E.K., Sinke, R.J., Rocchi, M., Marzella, R., Jenkins, N.A., Gilbert, D.J., Copeland, N.G.
Published in Genomics (San Diego, Calif.) (10.08.1995)
Published in Genomics (San Diego, Calif.) (10.08.1995)
Get full text
Journal Article
Assignment of the βB1 Crystallin Gene (CRYBB1) to Human Chromosome 22 and Mouse Chromosome 5
HULSEBOS, T.J.M., GILBERT, D.J., DELATTRE, O., SMINK, L.J., DUNHAM, I., WESTERVELD, A., THOMAS, G., JENKINS, N.A., COPELAND, N.G.
Published in Genomics (San Diego, Calif.) (10.10.1995)
Published in Genomics (San Diego, Calif.) (10.10.1995)
Get full text
Journal Article
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene
Bijlsma, E K, Merel, P, Fleury, P, van Asperen, C J, Westerveld, A, Delattre, O, Thomas, G, Hulsebos, T J
Published in Human genetics (01.07.1995)
Published in Human genetics (01.07.1995)
Get more information
Journal Article
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region
WIJKER, M, LIGTENBERG, M. J. L, LUNGAROTTI, M. S, ARWERT, F, SCHOUTE, F, DEFESCHE, J. C, PALS, G, BOLHUIS, P. A, ROPERS, H. H, HULSEBOS, T. J. M, MENKO, F. H, VAN OOST, B. A
Published in American journal of human genetics (01.05.1995)
Get full text
Published in American journal of human genetics (01.05.1995)
Journal Article