nvhg-nav.nl
Links
http://www.nvhg-nav.nl/links.aspx
De vereniging onderhoudt relaties met de volgende verenigingen en instanties:. De Federatie Medisch Biologische Verenigingen. De European Society of Human Genetics. De International Federation of Human Genetics Societies. Het International Congress of Human Genetics. Internationale humaan genetische organisaties. American Society of Human Genetics (ASHG). British Society for Human Genetics (BSHG). European Society of Human Genetics (ESHG). Genetics Society of America. German Society of Neurogenetics.
dridk.me
Naviguer dans le Génome humain // Sacha Schutz // bioinformatique génétique médecine
http://dridk.me/naviguer-dans-votre-adn.html
Naviguer dans le Génome humain. Dans ce post, nous allons voir comment naviguer dans le génome humain. Celui ci a été entièrement séquencé grâce à un consortium international de chercheurs au sein du. Entre 1990 et 2003. Ce génome fait environ 3 milliards de bases, soit un fichier texte d'environ 3 GigaOctets que vous pouvez télécharger ici. Aujourd'hui, le génome accompagné de ses annotations est disponible intégralement sur internet par l’intermédiaire de bases de données publiques. Il s'agit en fait, ...
humanvariomics.org
Types and quantities of variome - Humanvariomics.org
http://humanvariomics.org/index.php/Types_and_quantities_of_variome
Types and quantities of variome. The genetic variations comprise all de novo. Mutations and fixed variations. In the case of point mutation (change a single nucleotide for another), one showing fixation level over 1% in a population is called as SNP. When the de novo DNA variations are classified by the effect on genome structure, they can be categorized into small-scale variations and large-scale variations as follows,. 1 Small-scale variation affecting a small gene in one or a few nucleotides. Now let'...
ncbi.nlm.nih.gov
Cohen Syndrome - GeneReviews® - NCBI Bookshelf
http://www.ncbi.nlm.nih.gov/books/NBK1482
Skip to main content. Sign in to NCBI. NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health. Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Pagon RA, Adam MP, Ardinger HH, et al., editors. Seattle (WA): University of Washington, Seattle. MD, PhD, Marni J Falk. MD, Christine Wensel. MS, and Elias I Traboulsi. Clinical Geneticist, Division of Human Genetics. The diagnosis of Cohen s...
findbase.org
Documentation of pharmacogenomic markers allele frequencies
http://www.findbase.org/79-slideshow/77-at-vero-eos-et-accusamus-et-iusto-wisi-tincidunt
FINDbase.org - Genome Variation Allele Frequencies Database Worldwide. Thu, 13 Feb 2014 5pm. Gene and Mutation Map. Submit Genetic Disease Summaries. Documentation of causative mutations allele frequencies. Documentation of pharmacogenomic markers allele frequencies. Key project of the Genomic Medicine Alliance Genome Informatics Working Group. Innovative database structure and software design. Part of various European projects and International consortia. Innovative database structure and software design.
gest.org.tw
台灣消化系醫學會|The Gastroenterological Society of Taiwan
http://www.gest.org.tw/magazine
The Gastroenterological Society of Taiwan. Emsp; 聯絡我們. Emsp; English. Authorship and Conflicts of Interest Statement. Authors are welcome to submit reviews, perspectives, original articles, short communications, case reports, images and challenge, and letters to the editor for consideration. These Instructions to Authors are revised periodically by the Editors as needed. Authors should consult a recent issue of the Journal or visit http:/ www.aidm-online.com. Manuscripts (meaning all submission items...
findbase.org
Documentation of causative mutations allele frequencies
http://www.findbase.org/79-slideshow/88-consectetuer-cursus-dignissim-porttitor
FINDbase.org - Genome Variation Allele Frequencies Database Worldwide. Thu, 13 Feb 2014 5pm. Gene and Mutation Map. Submit Genetic Disease Summaries. Documentation of causative mutations allele frequencies. Documentation of pharmacogenomic markers allele frequencies. Key project of the Genomic Medicine Alliance Genome Informatics Working Group. Innovative database structure and software design. Part of various European projects and International consortia. Innovative database structure and software design.
findbase.org
Part of various European projects and International consortia
http://www.findbase.org/79-slideshow/79-mophie-and-intuit-launch-credit-card-processing
FINDbase.org - Genome Variation Allele Frequencies Database Worldwide. Thu, 13 Feb 2014 5pm. Gene and Mutation Map. Submit Genetic Disease Summaries. Documentation of causative mutations allele frequencies. Documentation of pharmacogenomic markers allele frequencies. Key project of the Genomic Medicine Alliance Genome Informatics Working Group. Innovative database structure and software design. Part of various European projects and International consortia. Innovative database structure and software design.
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