Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

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A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.

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Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

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http://www.wikidata.org/entity/Q35971326

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Application of a New Genetic D ...... Mutations in the Deaf in China

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Application of a New Genetic D ...... Mutations in the Deaf in China

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Application of a New Genetic D ...... Mutations in the Deaf in China

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Application of a New Genetic D ...... Mutations in the Deaf in China

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Application of a New Genetic D ...... Mutations in the Deaf in China

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Application of a New Genetic D ...... Mutations in the Deaf in China

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P1476

Application of a New Genetic D ...... Mutations in the Deaf in China

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P2093

Chang Hu

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

Chang Liu

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

Chufeng He

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

Hong Wu

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

Hongsheng Chen

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

Lingyun Mei

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

Lu Jiang

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

Qian Pan

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Xueming Liu

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

Yalan Liu

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P2860

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium

High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.

Genotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice.

Benefits of early intervention for children with hearing loss.

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

Field guide to next-generation DNA sequencers.

PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1

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scholarly article

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10.1371/JOURNAL.PONE.0151909

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English

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2016-03-28T00:00:00Z

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27018795

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4809548

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Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

about

P2860

P2860

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932