about
Predictive Value of GJB2 Mutation Status for Hearing Outcomes of Pediatric Cochlear Implantation.GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss.The Role of MicroRNAs in Environmental Risk Factors, Noise-Induced Hearing Loss, and Mental Stress.Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss.Cochlear Gene Therapy for Sensorineural Hearing Loss: Current Status and Major Remaining Hurdles for Translational Success.X-Linked Sensorineural Hearing Loss: A Literature Review
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016 թուականին հրատարակուած գիտական յօդուած
@hyw
2016 թվականին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
name
Genetics of Nonsyndromic Congenital Hearing Loss
@ast
Genetics of Nonsyndromic Congenital Hearing Loss
@en
Genetics of Nonsyndromic Congenital Hearing Loss
@nl
type
label
Genetics of Nonsyndromic Congenital Hearing Loss
@ast
Genetics of Nonsyndromic Congenital Hearing Loss
@en
Genetics of Nonsyndromic Congenital Hearing Loss
@nl
prefLabel
Genetics of Nonsyndromic Congenital Hearing Loss
@ast
Genetics of Nonsyndromic Congenital Hearing Loss
@en
Genetics of Nonsyndromic Congenital Hearing Loss
@nl
P2860
P356
P1433
P1476
Genetics of Nonsyndromic Congenital Hearing Loss
@en
P2093
M Tayyar Kalcioglu
Oguz Kadir Egilmez
P2860
P304
P356
10.1155/2016/7576064
P407
P577
2016-01-01T00:00:00Z