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Deletions in the genomes of fifteen inbred mouse lines and their possible implications for fat accumulation

Copy number variants (CNVs) are pieces of genomic DNA of 1000 base pairs or longer which occur in a given genome at a different frequency than in a reference genome. Their importance as a source for phenotypic variability has been recognized only in the last couple of years. Chromosomal deletions ca...

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Hlavní autoři: Schmitt, Armin O., Dempfle, Astrid, Brockmann, Gudrun A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Zhejiang University Press 2007
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2064947/
https://ncbi.nlm.nih.gov/pubmed/17973337
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.2007.B0777
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