Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.
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Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-AnalysisA novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2.Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous RegionHome-based Early Intervention on Auditory and Speech Development in Mandarin-speaking Deaf Infants and Toddlers with Chronological Aged 7-24 Months.A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China.Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaA reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan AssayDeveloping regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum.DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System.Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.
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P2860
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 17 December 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
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Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
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type
label
Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
@en
Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
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prefLabel
Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
@en
Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
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P2093
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Genetic mutations in nonsyndro ...... ethnicities in Yunnan, China.
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Dongyi Han
Guojian Wang
Jiandong Zhao
Mingyu Han
Xiaoming Deng
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P2888
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10.1186/1479-5876-11-312
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2013-12-17T00:00:00Z
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P6179
1008054977