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GENETIC ASSOCIATION ANALYSIS OF COPY NUMBER VARIATION (CNVs) IN HUMAN DISEASE PATHOGENESIS

Structural genetic variation, including copy number variation (CNV), constitutes a substantial fraction of total genetic variability and the importance of structural genetic variants in modulating human disease is increasingly being recognized. Early successes in identifying disease-associated CNVs...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Ionita-Laza, Iuliana, Rogers, Angela J., Lange, Christoph, Raby, Benjamin A., Lee, Charles
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2008
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2631358/
https://ncbi.nlm.nih.gov/pubmed/18822366
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygeno.2008.08.012
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