Publication Date:
2008-11-08
Description:
An ambitious plan to collect, curate, and make accessible information on genetic variations affecting human health is beginning to be realized.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810956/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810956/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cotton, Richard G H -- Auerbach, Arleen D -- Axton, Myles -- Barash, Carol Isaacson -- Berkovic, Samuel F -- Brookes, Anthony J -- Burn, John -- Cutting, Garry -- den Dunnen, Johan T -- Flicek, Paul -- Freimer, Nelson -- Greenblatt, Marc S -- Howard, Heather J -- Katz, Michael -- Macrae, Finlay A -- Maglott, Donna -- Moslein, Gabriela -- Povey, Sue -- Ramesar, Rajkumar S -- Richards, Carolyn S -- Seminara, Daniela -- Smith, Timothy D -- Sobrido, Maria-Jesus -- Solbakk, Jan Helge -- Tanzi, Rudolph E -- Tavtigian, Sean V -- Taylor, Graham R -- Utsunomiya, Joji -- Watson, Michael -- R37 DK044003/DK/NIDDK NIH HHS/ -- R37 DK044003-19/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2008 Nov 7;322(5903):861-2. doi: 10.1126/science.1167363.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Genomic Disorders Research Centre, Howard Florey Institute, Melbourne, Australia. cotton@unimelb.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18988827" target="_blank"〉PubMed〈/a〉
Keywords:
Databases, Factual
;
*Databases, Genetic
;
*Genetic Variation
;
*Genome, Human
;
Human Genome Project
;
Humans
;
Interdisciplinary Communication
;
International Cooperation
;
*Mutation
;
Nervous System Diseases/*genetics
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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