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Authors :
Fu Y; National Clinical Research Center for Otolaryngologic Diseases, College of Otolaryngology-Head and Neck Surgery, Sixth Medical Center of the PLA General Hospital, Beijing 100037, China Department of Otorhinolaryngology, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao 266035, China.; Huang SS
Subjects: Genetic Testing* ; Deafness*/Deafness*/Deafness*/genetics; Humans
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Source:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery [Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2024 Mar 07; Vol. 59 (3), pp. Publisher: Zhonghua yi xue hui za zhi she Country of Publication: China NLM ID: 101247574 Publication Model: Print Cited Medium: Print ISSN:
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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
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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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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
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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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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
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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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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
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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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Authors :
Zou Y; Department of Otolaryngology, Guangdong Women and Children Hospital, Guangzhou, 511400, China.; Dai QQ
Subjects: Genetic Testing* ; Mutation* ; Neonatal Screening*
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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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Authors :
Xie L; Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.; Qiu Y
Subjects: Genetic Testing* ; Mutation*; Deafness/Deafness/Deafness/*diagnosis
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Source:
Neural plasticity [Neural Plast] 2021 Jul 23; Vol. 2021, pp. 6151973. Date of Electronic Publication: 2021 Jul 23 (Print Publication: 2021).Publisher: Hindawi Pub. Corp Country of Publication: United States NLM ID: 100883417 Publication Model: eCollection Cited Medium: Internet ISSN:
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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
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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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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
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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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Authors :
Kim BJ; Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University Hospital, Seoul; †Department of Otorhinolaryngology-Head and Neck Surgery, Dankook University Hospital, Cheonan
Subjects: Deafness/Deafness/Deafness/*genetics ; Exome/Exome/Exome/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods
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Source:
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology [Otol Neurotol] 2015 Jul; Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 100961504 Publication Model: Print Cited Medium: Internet
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Authors :
Shaikh H; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.; Waryah AM
Subjects: Genetic Testing* ; Mutation* ; Phenotype*
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Source:
Biochemical genetics [Biochem Genet] 2017 Dec; Vol. 55 (5-6), pp. 410-420. Date of Electronic Publication: 2017 Oct 31.Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0126611 Publication Model: Print-Electronic Cited Medium:
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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
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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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