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Recent "Variation" articles

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Genes mirror geography within Europe
Nature, (2008)
 
Placement of cardiac electrodes: written, simulated, and actual accuracy.
J E Bupp et al.
American journal of critical care : an official publication, American Association of Critical-Care Nurses 6 (6), 457-62 (Nov 1997)
Posted by JLg100 to variation ECG on Mon Oct 06 2008 at 12:09 UTC | info | related
 
Accuracy in ECG lead placement among technicians, nurses, general physicians and cardiologists
R. Rajaganeshan et al.
International Journal of Clinical Practice 62 (1), 65-70 (2008)
Posted by JLg100 to variation ECG on Mon Oct 06 2008 at 12:08 UTC | info | related
 
Genome assembly comparison identifies structural variants in the human genome
Razi Khaja et al.
Nature Genetics, published online 22 Nov 2006
Posted by rkhaja (who is an author) and 7 others to variation on Mon Sep 29 2008 at 00:26 UTC | info | related
 
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
J Zhang et al.
Cytogenetic and genome research 115 (3-4), 205-14 (2006)
Posted by rkhaja (who is an author) and 1 other to variation on Mon Sep 29 2008 at 00:08 UTC | info | related
 
Making a Living as a Public Speaker
articlelux.com, (27 Sep 2008)
The wonderful dearly departed comic Chris Farley had a character that was a professional motivational speaker. That character was Matt Foley and he was an absolute mess. His speaking style was painful and destructive and he lived (say it with me) in a van down by the river. Well, as hilarious as [...]
 
Copy Number Variants and Segmental Duplications Show Different Formation Signatures - Google Search
www.google.com
Posted by quantuman to variation Structural on Mon Sep 22 2008 at 18:02 UTC | info | related
 
Integrated detection and population-genetic analysis of SNPs and copy number variation
Steven McCarroll et al.
Nat Genet 40 (10), 1166-74 (Oct 2008)
 
Medline search engine for finding genetic markers with biological significance.
Medline Search Engine for Finding Genetic Markers with Biological Significance
Weijian Xuan et al.
Bioinformatics (Oxford, England) 23 (18), 2477-84 (06 Sep 2007)
Tests using published data suggest MarkerInfoFinder can significantly increase the efficiency of finding genetic disorders and their underlying molecular mechanisms. The functions we developed will also be used to build a knowledge base for genetic markers and diseases.
 
Variations in DNA elucidate molecular networks that cause disease
Yanqing Chen et al.
Nature 452 (7186), 429-35 (16 Mar 2008)

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