Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns.
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Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss.A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides?A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.
P2860
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns.
description
2013 nî lūn-bûn
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2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
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2013年學術文章
@zh-hant
name
Combination of hearing screeni ...... ceptibility genes in newborns.
@en
Combination of hearing screeni ...... ceptibility genes in newborns.
@nl
type
label
Combination of hearing screeni ...... ceptibility genes in newborns.
@en
Combination of hearing screeni ...... ceptibility genes in newborns.
@nl
prefLabel
Combination of hearing screeni ...... ceptibility genes in newborns.
@en
Combination of hearing screeni ...... ceptibility genes in newborns.
@nl
P2093
P2860
P356
P1476
Combination of hearing screeni ...... ceptibility genes in newborns.
@en
P2093
Cai-Xia Sun
Ding-Li Chen
Gen-Dong Yao
Hai-Qin Feng
Shou-Xia Li
Su-Bin Zhao
Wei-Yong Zhang
Xiao-Fang Zhang
Yong-Jie Liu
P2860
P304
P356
10.3892/ETM.2013.1406
P577
2013-11-12T00:00:00Z