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Academic Journal

Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program.

  • Authors : Ruan Y; Otolaryngology-Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.

Subjects: Genetic Testing*/Genetic Testing*/Genetic Testing*/methods ; Deafness*/Deafness*/Deafness*/genetics ; Deafness*/Deafness*/Deafness*/diagnosis

  • Source: Bioscience trends [Biosci Trends] 2024 Sep 16; Vol. 18 (4), pp. 303-314. Date of Electronic Publication: 2024 Aug 25.Publisher: International Research and Cooperation Association for Bio & Socio-Sciences Advancement Country of Publication: Japan NLM ID: 101502754 Publication

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Correspondence on "The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review" by Freeman et al.

  • Authors : Li J; Medical Genetics Center, Lanzhou Maternal and Child Health Hospital, Gansu, China.; Sun X

Subjects: Genetic Testing* ; Deafness*/Deafness*/Deafness*/diagnosis ; Deafness*/Deafness*/Deafness*/genetics

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Jan; Vol. 25 (1), pp. 155-156. Date of Electronic Publication: 2022 Nov 14.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review.

  • Authors : Freeman L; School of Women's and Children's Health, Medicine, UNSW, Randwick, New South Wales, Australia; Graduate School of Health, University of Technology Sydney, Sydney, New South Wales, Australia.

Subjects: Deafness*/Deafness*/Deafness*/diagnosis ; Deafness*/Deafness*/Deafness*/genetics ; Genetic Testing*Nonsyndromic Deafness

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2022 Sep; Vol. 24 (9), pp. 1803-1813. Date of Electronic Publication: 2022 Jun 03.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Personal utility of genomic sequencing for infants with congenital deafness.

  • Authors : Tutty E; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

Subjects: Genetic Testing* ; Genomics*; Deafness/Deafness/Deafness/*diagnosis

  • Source: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3634-3643. Date of Electronic Publication: 2021 Jun 29.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Suspension array-based deafness genetic screening in 53,033 Chinese newborns identifies high prevalence of 109 G>A in GJB2.

  • Authors : Zou Y; Department of Otolaryngology, Guangdong Women and Children Hospital, Guangzhou, 511400, China.; Dai QQ

Subjects: Genetic Testing* ; Mutation* ; Neonatal Screening*

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Nov; Vol. 126, pp. 109630. Date of Electronic Publication: 2019 Aug 07.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.

  • Authors : Zhang M; a Department of Otolaryngology-Head and Neck Surgery , Shandong Provincial ENT Hospital, Shandong Provincial ENT Hospital Affiliated to Shandong University , Jinan , P.R. China.; b Key Laboratory of Otorhinolaryngology, National Health Commission (Shandong University) , Jinan , P.R. China.

Subjects: Deafness/Deafness/Deafness/*epidemiology ; Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods Nonsyndromic Deafness

  • Source: Acta oto-laryngologica [Acta Otolaryngol] 2019 Jul; Vol. 139 (7), pp. 612-617. Date of Electronic Publication: 2019 May 20.Publisher: Taylor & Francis Country of Publication: England NLM ID: 0370354 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials.

  • Authors : Chen S; Health Care Dept, Guangdong Women and Children's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.; Liang Z

Subjects: Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*statistics & numerical data; Asian People/Asian People/Asian People/genetics

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Jun; Vol. 121, pp. 99-108. Date of Electronic Publication: 2019 Mar 08.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Comprehensive Genetic Testing for Deafness from Fresh and Archived Dried Blood Spots.

  • Authors : Shearer AE; Department of Otolaryngology-Head and Neck Surgery, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.; Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.

Subjects: Deafness/Deafness/Deafness/*blood ; Deafness/Deafness/Deafness/*diagnosis ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery [Otolaryngol Head Neck Surg] 2018 Dec; Vol. 159 (6), pp. 1058-1060. Publisher: Wiley Country of Publication: England NLM ID: 8508176 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6817

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Academic Journal

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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Academic Journal

Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.

  • Authors : Wener ER; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; McLennan JD

Subjects: High-Throughput Nucleotide Sequencing* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/epidemiology

  • Source: The Laryngoscope [Laryngoscope] 2024 Aug; Vol. 134 (8), pp. 3832-3838. Date of Electronic Publication: 2024 Mar 01.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8607378 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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