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Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.

• Authors : Hao Z; Institute of Genomic and Personalized Medicine, College of Life Science, Huazhong University of Science and Technology, Wuhan, Hubei, China.; Fu D

Subjects: Mutation*; Connexins/Connexins/Connexins/*genetics ; Deafness/Deafness/Deafness/*diagnosis

• Source: PloS one [PLoS One] 2018 Apr 10; Vol. 13 (4), pp. e0195740. Date of Electronic Publication: 2018 Apr 10 (Print Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach.

• Authors : Yan D; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, United States of America.; Xiang G

Subjects: Oligonucleotide Array Sequence Analysis*/Oligonucleotide Array Sequence Analysis*/Oligonucleotide Array Sequence Analysis*/instrumentation; DNA/DNA/DNA/*metabolism ; Deafness/Deafness/Deafness/*genetics

• Source: PloS one [PLoS One] 2017 Mar 08; Vol. 12 (3), pp. e0169219. Date of Electronic Publication: 2017 Mar 08 (Print Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study.

• Authors : Palmer CG; Department of Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California, United States of America; Department of Human Genetics, University of California Los Angeles, Los Angeles, California, United States of America

Subjects: Genetic Counseling* ; Genetic Testing*; Connexins/Connexins/Connexins/*genetics

• Source: PloS one [PLoS One] 2014 Nov 06; Vol. 9 (11), pp. e111512. Date of Electronic Publication: 2014 Nov 06 (Print Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center.

• Authors : Wu CC; Department of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.; Hung CC

Subjects: Hospitals*; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis

• Source: PloS one [PLoS One] 2011; Vol. 6 (7), pp. e22314. Date of Electronic Publication: 2011 Jul 19.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

• Authors : Mori, Kentaro; Moteki, Hideaki; Miyagawa, Maiko

• Source: PLoS ONE. September 14, 2016, Vol. 11 Issue 9, e0162230

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Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS

• Authors : Miyagawa, Maiko; Nishio, Shin-ya; Ikeda, Takuo

• Source: PLoS ONE. October 9, 2013, Vol. 8 Issue 10, e75793

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Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients.

• Authors : Miyagawa, Maiko; Naito, Takehiko; Nishio, Shin-ya

Subjects: DEAFNESS; EXONS (Genetics); NUCLEOTIDE sequence

• Source: PLoS ONE; Aug2013, Vol. 8 Issue 8, p1-11, 11p

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Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness.

• Authors : Riahi, Zied; Bonnet, Crystel; Zainine, Rim

Subjects: GENETICS of deafness; GENETIC testing; RNA sequencing

• Source: PLoS ONE; Jun2014, Vol. 9 Issue 6, p1-6, 6p

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Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating.

• Authors : Qing, Jie; Yan, Denise; Zhou, Yuan

Subjects: GENETICS of deafness; LOCUS (Genetics); RIBOSOMAL RNA

• Source: PLoS ONE; Oct2014, Vol. 9 Issue 10, p1-8, 8p

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Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.

• Authors : Atik, Tahir; Onay, Huseyin; Aykut, Ayca

Subjects: HEARING disorders; GENETIC testing; GENETIC disorders

• Source: PLoS ONE; 11/11/2015, Vol. 10 Issue 10, p1-11, 11p

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