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Cytogenetics and Cell Genetics|January 1, 1991
Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2T J Hulsebos, E K Bijlsma, A H Geurts van Kessel, et al.International Journal of Cancer|May 16, 1998
Genetic sub-types of human malignant astrocytoma correlate with survivalS Leenstra, N T Oskam, E H Bijleveld, et al.Human Genetics|July 1, 1991
New distal marker closely linked to the fragile X locusT J Hulsebos, B A Oostra, S Broersen, et al.British Journal of Cancer|October 1, 1994
Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosisS Leenstra, E K Bijlsma, D Troost, et al.Genes, Chromosomes & Cancer|September 1, 1994
Analysis of mutations in the SCH gene in schwannomasE K Bijlsma, P Merel, D A Bosch, et al.Genes, Chromosomes & Cancer|April 1, 1997
Malignant astrocytoma-derived region of common amplification in chromosomal band 17p12 is frequently amplified in high-grade osteosarcomasT J Hulsebos, E H Bijleveld, N T Oskam, et al.Human Genetics|July 1, 1995
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 geneE K Bijlsma, P Merel, P Fleury, et al.Genes, Chromosomes & Cancer|August 1, 1995
Molecular analysis of genetic changes in ependymomasE K Bijlsma, A M Voesten, E H Bijleveld, et al.Genes, Chromosomes & Cancer|October 1, 1993
Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2E K Bijlsma, O Delattre, J A Juyn, et al.European Journal of Human Genetics : EJHG|April 26, 2000
Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22M Luijten, Y Wang, B T Smith, et al.Pageof 4