Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening. - Wikidata - wikimedia - TriplyDB

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

http://www.wikidata.org/entity/Q33312492

about

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss An automated microfluidic system for single-stranded DNA preparation and magnetic bead-based microarray analysis.Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region Rapid and Reliable Detection of Nonsyndromic Hearing Loss Mutations by Multicolor Melting Curve Analysis.Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss.The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age.Impact of gene patents and licensing practices on access to genetic testing for hearing loss.Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family.Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct.One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR.A rapid automatic processing platform for bead label-assisted microarray analysis: application for genetic hearing-loss mutation detection.Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.A universal multiplex PCR strategy for 100-plex amplification using a hydrophobically patterned microarray.A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family.

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Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening.

http://www.wikidata.org/entity/Q33312492

description

2008 nî lūn-bûn

@nan

2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2008年の論文

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2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

Construction of a multiplex al ...... ion to hearing loss screening.

@ast

Construction of a multiplex al ...... ion to hearing loss screening.

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Construction of a multiplex allele-specific PCR-based universal array

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type

label

Construction of a multiplex al ...... ion to hearing loss screening.

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Construction of a multiplex al ...... ion to hearing loss screening.

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Construction of a multiplex allele-specific PCR-based universal array

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Construction of a multiplex al ...... ion to hearing loss screening.

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Construction of a multiplex al ...... ion to hearing loss screening.

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Construction of a multiplex allele-specific PCR-based universal array

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Construction of a multiplex al ...... ion to hearing loss screening.

@en

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Cai-Xia Li

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Di Zhang

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

Hao Hu

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

Hua-Fang Gao

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

Jing Cheng

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Keith Mitchelson

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Kun Xia

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Pu Dai

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Qian Pan

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Wan-Li Xing

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P2860

Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement

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306-314

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scholarly article

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10.1002/HUMU.20622

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2

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29

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2008-02-01T00:00:00Z

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18161878

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