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Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns
Copy number variation (CNV) analysis has had a major impact on the field of medical genetics, providing a mechanism to identify disease-causing genomic alterations in an unprecedented number of diseases and phenotypes. CNV analysis is now routinely used in the clinical diagnostic laboratory, and has...
Tallennettuna:
| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3580449/ https://ncbi.nlm.nih.gov/pubmed/23114084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm381 |
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