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dc.contributorEconomy Divisionen_US
dc.contributor.authorUnited Nations Environment Programmeen_US
dc.contributor.authorWorld Health Organizationen_US
dc.contributor.authorInternational Labour Organisationen_US
dc.coverage.spatialGlobalen_US
dc.date.accessioned2019-08-20T20:30:26Z
dc.date.available2019-08-20T20:30:26Z
dc.date.issued1985
dc.identifier.isbn92 4 150186 5en_US
dc.identifier.urihttps://wedocs.unep.org/20.500.11822/29524
dc.descriptionThe extent to which human somatic and germinal mutation frequencies may be increased by exposure to ionizing radiation and to the variety of chemicals that characterize modern societies has been a matter of concern in recent years. Somatic mutations, either genic or chromosomal, are not transmitted to the offspring of an exposed individual. However, increases in the frequency of these mutations may contribute to an increase in the frequency of acquired disorders, for example, cancer. Increases in the frequency of germinal mutations, genic or chromosomal, are likely to contribute to inherited defects in the offspring of individuals exposed to mutagenic agents. There is, therefore, a clear need to develop and apply methods to study exposed populations at risk of increased levels of Somatic or germinal mutations.en_US
dc.formatTexten_US
dc.languageEnglishen_US
dc.rightsPublicen_US
dc.subjectGENETICSen_US
dc.subjectPOPULATIONen_US
dc.subjectEPIDEMIOLOGYen_US
dc.subjectMUTATIONen_US
dc.subjectCHROMOSOMESen_US
dc.subjectDEATHen_US
dc.subjectHEALTHen_US
dc.titleGuidelines for the Study of Genetic Effects in Human Populations - Environmental Health Criteria 46en_US


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