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Combined hearing screening and genetic screening of deafness among Hakka newborns in China.

• Authors : Zeng X; Laboratory of Medical Genetics, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China; Department of Clinical Laboratory, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China. Electronic address: .

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

• Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2020 Sep; Vol. 136, pp. 110120. Date of Electronic Publication: 2020 Jun 17.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Deafness induces complete crossmodal plasticity in a belt region of dorsal auditory cortex.

• Authors : Merrikhi, Yaser (AUTHOR); Mirzaei, Ali (AUTHOR); Kok, Melanie A. (AUTHOR)

Subjects: DEAFNESS; AUDITORY cortex; VISUAL perception

• Source: European Journal of Neuroscience. Aug2023, Vol. 58 Issue 4, p3058-3073. 16p. 1 Color Photograph, 1 Diagram, 5 Charts, 5 Graphs.

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Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.

• Authors : Kannan-Sundhari A; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, USA.; Dr. John T. Macdonald Foundation, Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.

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

• Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Oct; Vol. 24 (10), pp. 674-680. Date of Electronic Publication: 2020 Sep Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Genetic testing in the acute setting: a round table discussion.

• Authors : McDermott JH; Manchester Centre for Genomic, Manchester University NHS Foundation Trust, Manchester, UK .

Subjects: Hearing Loss*/Hearing Loss*/Hearing Loss*/chemically induced ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Point-of-Care Testing*

• Source: Journal of medical ethics [J Med Ethics] 2020 Aug; Vol. 46 (8), pp. 531-532. Date of Electronic Publication: 2020 Jul 10.Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 7513619 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

• Authors : DiStefano MT; ClinGen Hearing Loss Clinical Domain Working Group

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Oct; Vol. 21 (10), pp. 2239-2247. Date of Electronic Publication: 2019 Mar 21.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.

• Authors : Wang Q; Department of Otolaryngology-Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China.; Xiang J

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Neonatal Screening/Neonatal Screening/Neonatal Screening/*methods

• Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Oct; Vol. 21 (10), pp. 2231-2238. Date of Electronic Publication: 2019 Mar 20.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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New Research on Hearing Loss from National Institute on Deafness and Other Communication Disorders Summarized (Pathophysiology of human hearing loss associated with variants in myosins).

• Source: Health & Medicine Week. 2024, pages. 3943

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Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or Deafness.

• Authors : Bowden, Acacia; Hubbel, Alexandra; Smith, Lindsay

Subjects: GENETICS of deafness; COCHLEAR implants; SEQUENCE analysis

• Source: American Journal of Audiology. Mar2024, Vol. 33 Issue 1, p233-241. 9p.

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Education Full Text (H.W. Wilson)

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Detection of hereditary hearing loss gene by DNA microarray.

• Authors : Han GY; Xuzhou Institute of Medical Sciences, Xuzhou, Jiangsu, China. .; Xu Z

Subjects: Oligonucleotide Array Sequence Analysis*; Connexins/Connexins/Connexins/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

• Source: European review for medical and pharmacological sciences [Eur Rev Med Pharmacol Sci] 2017 Aug; Vol. 21 (16), pp. 3538-3542.Publisher: Verduci Country of Publication: Italy NLM ID: 9717360 Publication Model: Print Cited Medium: Internet ISSN: 2284-0729 (Electronic)

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