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Preimplantation genetic testing for hereditary hearing loss in Chinese population.

• Authors : Bi Q; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, National Clinical Research Center for Otolaryngologic Diseases, Key Lab of Hearing Impairment Science of Ministry of Education, Key Lab of Hearing Impairment Prevention and Treatment of Beijing, #28 Fuxing Road, Beijing, 100853, China.; Departments of Otolaryngology Head & Neck Surgery, China-Japan Friendship Hospital, 2#Yinghua Road, Beijing, 100029, China.

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

• Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2023 Jul; Vol. 40 (7), pp. 1721-1732. Date of Electronic Publication: 2023 Apr 05.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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[Using PGT to give birth to hereditary conductive deafness SYNS1 family a healthy offspring: a case report].

• 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

• 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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Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss.

• Authors : Jin X; National Research Institute for Family Planning, Beijing, China; National Human Genetic Resources Center, Beijing, China.

Subjects: CRISPR-Cas Systems*; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: European journal of medical genetics [Eur J Med Genet] 2022 Feb; Vol. 65 (2), pp. 104406. Date of Electronic Publication: 2021 Dec 27.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.

• Authors : Hu H; Second Affiliated Hospital, Army Military Medical University, Chongqing.; Zhou P

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

• Source: Medicine [Medicine (Baltimore)] 2021 Apr 30; Vol. 100 (17), pp. e25647.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN:

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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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Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families.

• Authors : Pandya A; Department of Pediatrics, Division of Genetics and Metabolism, UNC Chapel Hill, Chapel Hill, NC, USA.; O'Brien A

Subjects: Gene Deletion*; Connexin 30/Connexin 30/Connexin 30/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Apr; Vol. 8 (4), pp. e1171. Date of Electronic Publication: 2020 Feb 17.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 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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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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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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