High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

Autor:	Bruder, C E G, Hirvelä, Carina, Segraves, Richard, Wallace, Andrew J, Boltshauser, Eugene, Jordanova, Albena, Sainio, Markku, Harder, Henrik, Blennow, Elisabeth, Tapia-Paez, Isabel, Hamilton, Greg, Baser, Michael E, Papi, Laura, Rask-Andersen, Helge, Hung, Gene, Heiberg, Arvid, Albertson, Donna G, Fransson, Ingegerd, Zhang, Xiao Xiao, Zucman-Rossi6, Jessica, Rouleau, Guy A, Kluwe, Lan, Mathiesen, Tiit, Honda, Mariko, Pinkel, Daniel, Dumanski, Jan P, Evans, D Gareth, Hergersberg, Martin, Poptodorov, George, et al
Přispěvatelé:	University of Zurich, Bruder, C E G
Rok vydání:	2001
Předmět:	2716 Genetics (clinical) chromosomes acoustic neuroma 10039 Institute of Medical Genetics phenotype clone cells neoplasms 610 Medicine & health dna 142-005 142-005 neurofibromin 2 1311 Genetics pair 22 neurofibromatosis 2 1312 Molecular Biology human genes genome Genetics (clinical) heterozygote homozygote 10036 Medical Clinic 570 Life sciences biology mutation heterogeneity tumor suppressor genes autosome disorder
DOI:	10.5167/uzh-154313
Databáze:	OpenAIRE
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