British Society for Human Genetics
Founded in 1996, the British Society for Human Genetics is a forum for professionals working in all aspects of Human Genetics, from cutting edge research to the delivery of genetics services to the population of the UK.
European Society of Human Genetics
European Society of Human Genetics is an international professional organisation. Its site includes info about courses and conferences, links, and policy documents
GeneClinics is an expert-authored, peer-reviewed clinical genetic information resource consisting of concise descriptions of specific inherited disorders and authoritative, current information on the role of genetic testing in the diagnosis, management, and genetic counseling of patients with these inherited conditions.
GeneTests™ promotes the appropriate use of genetic counseling and genetic testing in patient care. GeneTests™ provides reliable, easy-to-use and current genetic counseling and testing information for the benefit of families and their healthcare providers.
Genome.gov National Human Genome Research Institute
Sponsored by The National Human Genome Research Institute (NHGRI) the streamlined Web site address makes it easy for users to access a comprehensive and authoritative government site focused on genomic research, including the international Human Genome Project. The Web site supports ongoing scientific studies by researchers inside and outside of the institute as well as providing a reliable source of genomic information for a wide range of audiences, including individuals with genetic disorders and their families, teachers and
students and the general public. Links on the home page connect users to other federal government sources for information about genomics.
Genome.gov All About The Human Genome Project (HGP)
The Human Genome Project (HGP) was one of the great feats of exploration in history - an inward voyage of discovery rather than an outward exploration of the planet or the cosmos; an international research effort to sequence and map all of the genes - together known as the genome - of members of our species, Homo sapiens. Completed in April 2003, the HGP gave us the ability to, for the first time, to read nature's complete genetic blueprint for building a human being.
Human Gene Mutation Database
The database is a comprehensive international database og genetic lesions that cause disease. The Human Gene Mutation Database constitutes the intellectual property of the University of Wales College of Medicine.
The information in HumGen is divided into three main areas. The current-awareness function of HumGen is served by GenInfo, which provides information such as recent statements and press releases. GenBiblio is a search engine that allows users to find and collate archived information. Finally, GenConnect provides contact information for over 200 organizations (governmental and non-governmental) that provide the statements that are made available at HumGen.
Office of Genetics and Disease Prevention, CDC
The Office of Genetics and Disease Prevention is the pioneer in public health genetics, The site includes papers and policy documents on public health aspects of genetics, a collection of links, and news
OMIM(TM), Online Mendelian Inheritance in Man Database
This database is a catalog of human genes and genetic disorders authored and edited by Dr. Victor A. McKusick and his colleagues at Johns Hopkins and elsewhere, and developed for the World Wide Web by NCBI, the National Center for Biotechnology Information. The database contains textual information, pictures, and reference information. It also contains copious links to NCBI's Entrez database of MEDLINE articles and sequence information.
PubCrawler - an Update Alerting Service for PubMed and GenBank
PubCrawler is a free "alerting" service that scans daily updates to the NCBI Medline (PubMed) and GenBank databases. PubCrawler can keep scientists informed of the current contents of Medline and GenBank, by listing new database entries that match their research interests.
The Sanger Centre
The Sanger Centre is a genome research centre founded by the Wellcome Trust and the Medical Research Council. Our purpose is to further the knowledge of genomes, particularly through large scale sequencing and analysis. Godt sted med masser af vigtig information om dette område. Fin site map letter oversigten.