High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

Deletions and amplifications of the human genomic sequence (copy number polymorphisms) are the cause of numerous diseases and a potential cause of phenotypic variation in the normal population. Comparative genomic hybridization (CGH) has been developed as a useful tool for detecting alterations in D...

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Bibliografiset tiedot
Päätekijät: Urban, Alexander Eckehart, Korbel, Jan O., Selzer, Rebecca, Richmond, Todd, Hacker, April, Popescu, George V., Cubells, Joseph F., Green, Roland, Emanuel, Beverly S., Gerstein, Mark B., Weissman, Sherman M., Snyder, Michael
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2006
Aiheet:
Biological Sciences
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1450206/
https://ncbi.nlm.nih.gov/pubmed/16537408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0511340103
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