数据链接：
官方服务：
资源简介：
GJB2 genotypes in patients with HI.
应用场景：
创建时间：
2016-05-26
相关数据集
Hearing Loss in a Mouse Model of 22q11.2 Deletion Syndrome
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.
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
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
Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis
Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian in
Figshare2016-01-18 更新60
Rare PCDH15 SNVs identified in this study.
Rare PCDH15 SNVs identified in this study.
Figshare2016-04-12 更新50
