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Rapid and Inexpensive Screening of Genomic Copy Number Variations Using a Novel Quantitative Fluorescent PCR Method

Detection of human microdeletion and microduplication syndromes poses significant burden on public healthcare systems in developing countries. With genome-wide diagnostic assays frequently inaccessible, targeted low-cost PCR-based approaches are preferred. However, their reproducibility depends on e...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Stofanko, Martin, Han, Joan C., Elsea, Sarah H., Pena, Heloísa B., Gonçalves-Dornelas, Higgor, Pena, Sérgio Danilo Junho
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3830787/
https://ncbi.nlm.nih.gov/pubmed/24288428
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/704917
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