Search Results - "CNV"

Characterising amylase gene CNVs and application to association studies by Shwan, Nzar Ali Ameen

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Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity by Carpenter, Danielle, Mitchell, Laura, Armour, John A.L.

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Recurrent rearrangements of human amylase genes create multiple independent CNV series by Shwan, Nzar A.A., Louzada, Sandra, Yang, Fengtang, Armour, John A.L.

Subjects: “…genomic mutation; adaptation; genomic instability; CNV…”
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Investigating association of predisposition genes as a risk of developing multifactorial diseases by Arginbekova, Assel

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Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus by Black, Holly A., Khan, Fayeza F., Tyson, Jess, Armour, John A.L.

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Peripheral hearing loss reduces the ability of children to direct selective attention during multi-talker listening by Holmes, Emma, Kitterick, Pádraig T., Summerfield, A. Quentin

Subjects: “…Hearing loss; Multi-talker listening; Auditory Attention; Spatial attention; EEG; CNV…”
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