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Moslein, G.

( G. Moslein)


cancer family chromosome sample breast mutation ratio breast cancer genomic array colorectal cancer ampli colorectal clone patient microdissected analysis fication array cgh genome figure tumor hybridization control change acids research genomic dna copy-number log 2 ratio log 2 ratios table genomic hybridization method microarray region cohort level number reference amplification deletion model meijers-heijboer amount hnpcc phenotype ampli fied copy-number changes study hnpcc-like disease detection colorectal cancer cases tissue genes chromosomes cancer chromosomal unampli research oligonucleotide approach 29-ampli result hbcc phenotype signi material criteria alteration sequence intercept age !60 years pilot genomic dna samples threshold breast cancer risk carrier genet mucosa resolution disease chromosome 5 chromosome x




2 Most Recent Publications

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH. (Article)
Cardoso, J. Molenaar, L. Menezes, R.X. de Rosenberg, C. Morreau, H. Moslein, G. Fodde, R. Boer, J.M.
2004-01-01
The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype (Article)
Meijers-Heijboer, E.J. Moslein, G. Bos, R.R. van den Snoo, A. de Schutte, A.E.M. Franken, P.F. Fat, G.T. Jagmohan, S. Chapman, P. Brekelmans, C.T. Wijnen, J. Vasen, H. Lynch, H. Ouweland, A.M.W. van den Klijn, J.G.M. Hollestelle, A. Wasielewski, M. Fodde, R. Wagner, A. Elstrodt, F. Verkuijlen, P. Tops, C. Burn, J.
2003-01-01