dc.creator | Wallace, Robert W. | en |
dc.date.accessioned | 2015-05-05T19:03:26Z | en |
dc.date.available | 2015-05-05T19:03:26Z | en |
dc.date.created | 1998-02 | en |
dc.date.issued | 1998-02 | en |
dc.identifier | 10.1016/S1357-4310(97)01206-9 | en |
dc.identifier.bibliographicCitation | Molecular Medicine Today. 1998 Feb; 4(2): 59-62. | en |
dc.identifier.issn | 1357-4310 | en |
dc.identifier.uri | http://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=The+Human+Genome+Diversity+Project:+Medical+Benefits+Versus+Ethical+concerns&title=Molecular+Medicine+Today.++&volume=4&issue=2&pages=59-62&date=1998&au=Wallace,+Robert+W. | en |
dc.identifier.uri | http://dx.doi.org/10.1016/S1357-4310(97)01206-9 | en |
dc.identifier.uri | http://hdl.handle.net/10822/754725 | en |
dc.description.abstract | By the year 2005 the entire human genome should have been sequenced
and the genes identified. But the resulting genomic sequence, although a
marvelous accomplishment, will be a composite of just a handful of individuals
selected at random. The Human Genome Diversity Project was proposed as a
means to overcome these limitations by obtaining genetic information from many
diverse populations of the world. This would give medical geneticists a handle
on the variations in susceptibility to disease among different populations, as
well as being of anthropological value. But would such a project risk
exploiting the indigenous populations involved? | en |
dc.format | Article | en |
dc.language | en | en |
dc.source | BRL:MEDKIE/98209011 | en |
dc.subject | Anthropology | en |
dc.subject | Consent | en |
dc.subject | Developing Countries | en |
dc.subject | Disease | en |
dc.subject | DNA | en |
dc.subject | DNA Data Banks | en |
dc.subject | Data Banks | en |
dc.subject | Ethical Review | en |
dc.subject | Federal Government | en |
dc.subject | Genes | en |
dc.subject | Genetic Diversity | en |
dc.subject | Genetic Information | en |
dc.subject | Genetic Research | en |
dc.subject | Genetics | en |
dc.subject | Genome | en |
dc.subject | Genome Mapping | en |
dc.subject | Government | en |
dc.subject | Government Financing | en |
dc.subject | Guidelines | en |
dc.subject | Health | en |
dc.subject | Human Genome | en |
dc.subject | Human Genome Diversity Project | en |
dc.subject | Indigenous Populations | en |
dc.subject | Industry | en |
dc.subject | Informed Consent | en |
dc.subject | International Aspects | en |
dc.subject | Patents | en |
dc.subject | Population Genetics | en |
dc.subject | Privacy | en |
dc.subject | Public Policy | en |
dc.subject | Research | en |
dc.subject | Review | en |
dc.subject | Risk | en |
dc.subject | Science | en |
dc.subject | Tissue Banks | en |
dc.title | The Human Genome Diversity Project: Medical Benefits Versus Ethical Concerns | en |
dc.provenance | Digital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine. | en |
dc.provenance | Digital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University. | en |