Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?

Strahlentherapie und Onkologie

Volumn 178, Issue 4, 2002, Pages 209-215

  Kuechler, Alma ^a   Neubauer, Susann ^b   Grabenbauer, Gerhard G ^b   Claussen, Uwe ^c   Liehr, Thomas ^c   Sauer, Rolf ^b   Wendt, Thomas G ^a  

^a Clinic of Radiology   (Germany)

^b Department of Radiotherapy ^*  (Germany)

^c Institute of Human Genetics and Anthropology   (Germany)

Author keywords

24 Color FISH; Individual radiosensitivity; NBS; Nijmegen breakage syndrome; Radiation induced chromosomal aberrations

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME PAINTING; CONTROLLED STUDY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; LYMPHOCYTE; RADIATION MUTAGENESIS; RADIOSENSITIVITY; RELIABILITY; SCHOOL CHILD;

ADULT; CELLS, CULTURED; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKAGE; CHROMOSOME PAINTING; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHOCYTES; MALE; METAPHASE; MIDDLE AGED; RADIATION DOSAGE; RADIATION TOLERANCE; SYNDROME;

EID: 0036223462     PISSN: 01797158     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00066-002-0904-0     Document Type: Article

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