22q11.2 Deletion Syndrome (22q11DS) arises from an interstitial chromosomal microdeletion encompassing at least 30 genes. This disorder is one of the most significant known cytogenetic risk factors fo

NIAID Data Ecosystem70

Genomic risk loci for hearing aid use.

遗传性听力障碍

全基因组关联分析

Loci were defined by the set of all SNPs in LD (r2 > 0.6, 1000 Genomes Phase 3 European samples) with an independently significant SNP (p < 5e-8) at that locus. Start and end refer to the left- and ri

NIAID Data Ecosystem50

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM® genes for hereditary disorders of hearing and balance. Xenopus laevis

遗传性听力障碍

比较转录组分析

Purpose: To identify orthologous genes in Xenopus that are implicated in deafness and vestibular disorders in humans and to compare RNA-Seq and microarray to determine the advantages of each technolog

NIAID Data Ecosystem40

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIMÂ® genes for hereditary disorders of hearing and balance

资源简介：

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIMÂ® genes for hereditary disorders of hearing and balance

资源简介：

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