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Copy number variation in chemokine superfamily: the complex scene of CCL3L–CCL4L genes in health and disease

Genome copy number changes (copy number variations: CNVs) include inherited, de novo and somatically acquired deviations from a diploid state within a particular chromosomal segment. CNVs are frequent in higher eukaryotes and associated with a substantial portion of inherited and acquired risk for v...

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Detaylı Bibliyografya
Asıl Yazarlar: Colobran, R, Pedrosa, E, Carretero-Iglesia, L, Juan, M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Blackwell Science Inc 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2990928/
https://ncbi.nlm.nih.gov/pubmed/20659124
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2249.2010.04224.x
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