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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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2006
Matèries:
Biological Sciences
Accés en línia: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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