Unbound MEDLINE

Articles related to 18787571 journal articles from PubMed MEDLINE database

Unbound MEDLINE results for:Bookmark this site
Articles related to 18787571 [Unique ID], provided by the PubMed system
1 - 10 of 115 journal articles in the PubMed databaseEmail to a friend    
 
Barøy T, Misceo D, Frengen E 
[Structural variation in the human genome contributes to variation of traits.] [JOURNAL ARTICLE]
Tidsskr Nor Laegeforen 2008 Sep 11; 128(17):1951-1955.
Abstract | Full Citation | Find Related Articles 
Feuk L, Carson AR, Scherer SW 
Structural variation in the human genome. [Journal Article, Review]
Nat Rev Genet 2006 Feb; 7(2):85-97.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Kidd JM, Cooper GM, Donahue WF, et al. 
Mapping and sequencing of structural variation from eight human genomes. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.]
Nature 2008 May 1; 453(7191):56-64.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Hinds DA, Kloek AP, Jen M, et al. 
Common deletions and SNPs are in linkage disequilibrium in the human genome. [Journal Article]
Nat Genet 2006 Jan; 38(1):82-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Reymond A, Henrichsen CN, Harewood L, et al. 
Side effects of genome structural changes. [Journal Article]
Curr Opin Genet Dev 2007 Oct; 17(5):381-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Cheung J, Estivill X, Khaja R, et al. 
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. [Journal Article]
Genome Biol 2003; 4(4):R25.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Wheeler DA, Srinivasan M, Egholm M, et al. 
The complete genome of an individual by massively parallel DNA sequencing. [Journal Article]
Nature 2008 Apr 17; 452(7189):872-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Bader JS 
The relative power of SNPs and haplotype as genetic markers for association tests. [Journal Article]
Pharmacogenomics 2001 Feb; 2(1):11-24.
Abstract | Full Citation | Publisher Full Text | Find Related Articles 
Beckmann JS, Estivill X, Antonarakis SE 
Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability. [Journal Article]
Nat Rev Genet 2007 Aug; 8(8):639-46.
Abstract | Full Citation | Find Related Articles 
New Search Next Results
  

Enter
www.unboundmedicine.com/medline
in your iPhone browser
or View our
Unbound MEDLINE
iPhone demo


Advertise on this site.