Deafness gene mutations in newborns in Beijing.

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Mitochondrial hearing loss mutations among Finnish preterm and term-born infants.

P2860

Q47114347-6DFDEF7E-9D18-4845-9C09-8E9B8D6CAAD8

P2860

Deafness gene mutations in newborns in Beijing.

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http://www.wikidata.org/entity/Q40109145

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2016 nî lūn-bûn

@nan

2016年の論文

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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

2016年學術文章

@zh

2016年學術文章

@zh-hant

name

Deafness gene mutations in newborns in Beijing.

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Item

label

Deafness gene mutations in newborns in Beijing.

@en

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Deafness gene mutations in newborns in Beijing.

@en

P1476

Deafness gene mutations in newborns in Beijing

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P2093

Adong Shen

http://www.w3.org/2001/XMLSchema#string

Fang Xu

http://www.w3.org/2001/XMLSchema#string

Haihong Liu

http://www.w3.org/2001/XMLSchema#string

Jie Lu

http://www.w3.org/2001/XMLSchema#string

Jin Shi

http://www.w3.org/2001/XMLSchema#string

Jinsheng Hao

http://www.w3.org/2001/XMLSchema#string

Ping Chu

http://www.w3.org/2001/XMLSchema#string

Shujing Han

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Xiaojian Yang

http://www.w3.org/2001/XMLSchema#string

Xin Ni

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P2860

SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age.

Genetic screening for deafness.

Deafness genes and their diagnostic applications.

Newborn hearing screening--a silent revolution.

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475-479

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scholarly article

P356

10.3109/00016489.2015.1128121

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English

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136

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Yaqiong Jin

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2016-01-14T00:00:00Z

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P698

26766211

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P921

Beijing

Deafness gene mutations in newborns in Beijing.

about

P2860

P2860

Deafness gene mutations in newborns in Beijing.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921