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Subject : genetic testing Subject : medical screening Geographic : china
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Academic Journal

[Analysis of results of concurrent hearing and deafness genetic screening and follow up of 33 911 newborns].

  • Authors : Lei J; Department of Clinical Laboratory, Shenzhen Nanshan Maternity and Child Health Care Hospital, Shenzhen, Guangdong 518067, China. .; Han L

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

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 32-36.Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print

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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

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

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

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

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 Publication: 2018).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Detecting novel mutations and combined Klinefelter syndrome in Usher syndrome cases.

  • Authors : Li X; a Department of Otolaryngology, Head and Neck Surgery , Chinese PLA General Hospital , Beijing , PR China.; Huang S

Subjects: Genetic Predisposition to Disease*; Deafness/Deafness/Deafness/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: Acta oto-laryngologica [Acta Otolaryngol] 2019 Jun; Vol. 139 (6), pp. 479-486. Date of Electronic Publication: 2019 Apr 29.Publisher: Taylor & Francis Country of Publication: England NLM ID: 0370354 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic screening involving 101 hot spots for neonates not passing newborn hearing screening and those random recruited in Dongguan.

  • Authors : Liu Y; Department of Prenatal Diagnosis Center, Dongguan Maternal and Child Health Hospital, Dongguan 523112, Guangdong, China.; Ye L

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

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2019 Feb; Vol. 117, pp. 82-87. Date of Electronic Publication: 2018 Nov 22.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach.

  • Authors : Wang J; Department of Obstetrics and Gynecology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230001, Anhui, China.; Xiang J

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

  • Source: Scientific reports [Sci Rep] 2021 Feb 17; Vol. 11 (1), pp. 4036. Date of Electronic Publication: 2021 Feb 17.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

[Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis].

  • Authors : Lyu K; Chengdu Women's & Children's Central Hospital, Chengdu, Sichuan 610091, P.R.China. .; Xiong Y

Subjects: Mutation*; Deafness/Deafness/Deafness/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

  • Source: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2014 Oct; Vol. 31 (5), pp. 547-52.Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print

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  • 1-10 of  94 results for ""Deafness""