Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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P1476

Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.

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P2093

Hao Wu

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Longxia He

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Penghui Chen

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Tao Yang

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Xiaowen Wang

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Xiuhong Pang

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P2860

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Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.

Identification of sequence variants in genetic disease-causing genes using targeted next-generation sequencing.

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.

Genetic epidemiology of hearing impairment.

P2888

s41598-017-10099-2

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scholarly article

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10.1038/S41598-017-10099-2

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English

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P577

2017-09-12T00:00:00Z

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28900111

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5595904

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