Hereditary hearing loss SNP-microarray pilot study

OBJECTIVES: Despite recent advancements in diagnostic tools, the genomic landscape of hereditary hearing loss remains largely uncharacterized. One strategy to understand genome-wide aberrations includes the analysis of copy number variation that can be mapped using SNP-microarray technology. A growi...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:BMC Res Notes
Päätekijät: Vona, Barbara, Hofrichter, Michaela A. H., Schröder, Jörg, Shehata-Dieler, Wafaa, Nanda, Indrajit, Haaf, Thomas
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
Aiheet:
Data Note
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6003021/
https://ncbi.nlm.nih.gov/pubmed/29903040
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-018-3466-7
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