Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening (Q33312492)

25 July 2017

title

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

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25 July 2017

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Cai-Xia Li

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25 July 2017

Qian Pan

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25 July 2017

Yong-Gang Guo

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25 July 2017

Yan Li

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25 July 2017

Hua-Fang Gao

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25 July 2017

Di Zhang

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25 July 2017

Hao Hu

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25 July 2017

Wan-Li Xing

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25 July 2017

Keith Mitchelson

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25 July 2017

Kun Xia

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25 July 2017

Pu Dai

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25 July 2017

Jing Cheng

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25 July 2017

publication date

1 February 2008

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25 July 2017

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25 July 2017

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25 July 2017

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25 July 2017

page(s)

306-314

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

25 July 2017

cites work

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Crossref

https://api.crossref.org/works/10.1002%2FHUMU.20622

Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2).

21 January 2018

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Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan

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12 December 2020

Scanometric DNA Array Detection with Nanoparticle Probes

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Detection of mutations in genes associated with hearing loss using a microarray-based approach

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Sensitive detection of SARS coronavirus RNA by a novel asymmetric multiplex nested RT-PCR amplification coupled with oligonucleotide microarray hybridization

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12 December 2020

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

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12 December 2020

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

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12 December 2020

Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up

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12 December 2020

Development of a genotyping microarray for Usher syndrome

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12 December 2020

Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness

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12 December 2020

Multiplexed genotyping with sequence-tagged molecular inversion probes

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12 December 2020

Genetic epidemiology of hearing impairment

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12 December 2020

Prevalent connexin 26 gene (GJB2) mutations in Japanese

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12 December 2020

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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12 December 2020

Identification of APC gene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization

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12 December 2020

Genotyping for platelet-specific antigens: techniques for the detection of single nucleotide polymorphisms

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12 December 2020

A microsphere-based assay for multiplexed single nucleotide polymorphism analysis using single base chain extension

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12 December 2020

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

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12 December 2020

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese

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12 December 2020

Genomic analysis of anti-hepatitis B virus (HBV) activity by small interfering RNA and lamivudine in stable HBV-producing cells

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12 December 2020

Human Nonsyndromic Sensorineural Deafness

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12 December 2020

Rapid and comprehensive determination of cytochrome P450 CYP2D6 poor metabolizer genotypes by multiplex polymerase chain reaction

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12 December 2020

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

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12 December 2020

Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss

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12 December 2020

Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins

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12 December 2020

Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: a single-step approach

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12 December 2020

Multiplex analysis of the most common mutations related to hereditary haemochromatosis: two methods combining specific amplification with capillary electrophoresis

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12 December 2020

Universal DNA microarray method for multiplex detection of low abundance point mutations

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12 December 2020

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

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12 December 2020

Development of miniaturized competitive immunoassays on a protein chip as a screening tool for drugs

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12 December 2020

Proteomic fingerprints for potential application to early diagnosis of severe acute respiratory syndrome

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12 December 2020

Direct haplotype determination by double ARMS: specificity, sensitivity and genetic applications

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12 December 2020

A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

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12 December 2020

Identifiers

DOI

10.1002/HUMU.20622

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release_phjbbitcpfgxjnqmiqtt6efbdy

25 July 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/phjbbitcpfgxjnqmiqtt6efbdy

24 November 2022

mapped directly with Wikidata item

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