155 related articles for article (PubMed ID: 38767670)
21. A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.
Azadegan-Dehkordi F; Ahmadi R; Bahrami T; Yazdanpanahi N; Farrokhi E; Tabatabaiefar MA; Hashemzadeh-Chaleshtori M
Am J Otolaryngol; 2018; 39(6):719-725. PubMed ID: 30077349
[TBL] [Abstract][Full Text] [Related]
22. Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China.
Hu H; Zhou P; Wu J; Lei W; Wang Y; Yang Y; Liu H
Medicine (Baltimore); 2021 Apr; 100(17):e25647. PubMed ID: 33907123
[TBL] [Abstract][Full Text] [Related]
23. Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
Wang R; Han S; Khan A; Zhang X
Genet Test Mol Biomarkers; 2017 May; 21(5):316-321. PubMed ID: 28281779
[TBL] [Abstract][Full Text] [Related]
24. Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.
Noman M; Ishaq R; Bukhari SA; Ahmed ZM; Riazuddin S
Genes (Basel); 2019 Dec; 10(12):. PubMed ID: 31835641
[TBL] [Abstract][Full Text] [Related]
25. MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance.
Thongpradit S; Jinawath N; Javed A; Noojarern S; Khongkraparn A; Tim-Aroon T; Lertsukprasert K; Suktitipat B; Jensen LT; Wattanasirichaigoon D
Sci Rep; 2020 Jul; 10(1):12712. PubMed ID: 32728090
[TBL] [Abstract][Full Text] [Related]
26. Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF.
Khalil A; Karroum SB; Barake R; Dunya G; Abou-Rizk S; Kamar A; Nemer G; Bassim M
BMC Med Genet; 2020 Jan; 21(1):1. PubMed ID: 31898538
[TBL] [Abstract][Full Text] [Related]
27. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.
Bitarafan F; Seyedena SY; Mahmoudi M; Garshasbi M
J Clin Lab Anal; 2020 Dec; 34(12):e23544. PubMed ID: 32864763
[TBL] [Abstract][Full Text] [Related]
28. Challenges and solutions for gene identification in the presence of familial locus heterogeneity.
Rehman AU; Santos-Cortez RL; Drummond MC; Shahzad M; Lee K; Morell RJ; Ansar M; Jan A; Wang X; Aziz A; Riazuddin S; Smith JD; Wang GT; Ahmed ZM; Gul K; Shearer AE; Smith RJ; Shendure J; Bamshad MJ; Nickerson DA; ; Hinnant J; Khan SN; Fisher RA; Ahmad W; Friderici KH; Riazuddin S; Friedman TB; Wilch ES; Leal SM
Eur J Hum Genet; 2015 Sep; 23(9):1207-15. PubMed ID: 25491636
[TBL] [Abstract][Full Text] [Related]
29. Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.
Woo HM; Park HJ; Baek JI; Park MH; Kim UK; Sagong B; Koo SK
BMC Med Genet; 2013 Jul; 14():72. PubMed ID: 23865914
[TBL] [Abstract][Full Text] [Related]
30. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D
Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623
[TBL] [Abstract][Full Text] [Related]
31. Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.
Yazdanpanahi N; Chaleshtori MH; Tabatabaiefar MA; Noormohammadi Z; Farrokhi E; Najmabadi H; Shahbazi S; Hosseinipour A
Int J Pediatr Otorhinolaryngol; 2012 Jun; 76(6):845-50. PubMed ID: 22444735
[TBL] [Abstract][Full Text] [Related]
32. Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.
Woo HM; Park HJ; Park MH; Kim BY; Shin JW; Yoo WG; Koo SK
BMC Med Genet; 2014 Apr; 15():46. PubMed ID: 24767429
[TBL] [Abstract][Full Text] [Related]
33. A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.
Ghasemnejad T; Shekari Khaniani M; Nouri Nojadeh J; Mansoori Derakhshan S
BMC Med Genomics; 2022 Feb; 15(1):18. PubMed ID: 35101039
[TBL] [Abstract][Full Text] [Related]
34. Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y; Tariq M; He S; Abdullah U; Zhang J; Baig SM
BMC Med Genet; 2020 Jul; 21(1):151. PubMed ID: 32682410
[TBL] [Abstract][Full Text] [Related]
35. Mutation spectrum of non-syndromic hearing loss in the UAE, a retrospective cohort study and literature review.
Elsayed O; Al-Shamsi A
Mol Genet Genomic Med; 2022 Nov; 10(11):e2052. PubMed ID: 36056583
[TBL] [Abstract][Full Text] [Related]
36. Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families.
Liu Y; Wen J; Sang S; Mei L; He C; Jiang L; Huang S; Feng Y
Eur Arch Otorhinolaryngol; 2020 Dec; 277(12):3331-3339. PubMed ID: 32447495
[TBL] [Abstract][Full Text] [Related]
37. Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani Kindred.
Saleem IB; Masoud MS; Qasim M; Ali M; Ahmed ZM
Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946889
[TBL] [Abstract][Full Text] [Related]
38. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.
Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM
Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923
[TBL] [Abstract][Full Text] [Related]
39. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang YB; Tang SH; Li HZ; Xu CY; Chen C; Xu YZ; Ding LR; Xu XQ
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():185-190. PubMed ID: 31035178
[TBL] [Abstract][Full Text] [Related]
40. Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).
Сhurbanov AY; Karafet TM; Morozov IV; Mikhalskaia VY; Zytsar MV; Bondar AA; Posukh OL
PLoS One; 2016; 11(4):e0153841. PubMed ID: 27082237
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
