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Detection limit of intragenic deletions with targeted array comparative genomic hybridization
BACKGROUND: Pathogenic mutations range from single nucleotide changes to deletions or duplications that encompass a single exon to several genes. The use of gene-centric high-density array comparative genomic hybridization (aCGH) has revolutionized the detection of intragenic copy number variations....
Tallennettuna:
| Julkaisussa: | BMC Genet |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4235222/ https://ncbi.nlm.nih.gov/pubmed/24304607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-14-116 |
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