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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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Detaylı Bibliyografya
Asıl Yazarlar: Schmitt, Armin O., Dempfle, Astrid, Brockmann, Gudrun A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Zhejiang University Press 2007
Konular:
Online Erişim: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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