These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
142 related articles for article (PubMed ID: 38860500)
1. Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants. Ma P; Zhou B; Kang Q; Chen X; Tian X; Hui L; Hao S; Wu H; Zhang C Mol Genet Genomic Med; 2024 Jun; 12(6):e2434. PubMed ID: 38860500 [TBL] [Abstract][Full Text] [Related]
2. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing. Safka Brozkova D; Poisson Marková S; Mészárosová AU; Jenčík J; Čejnová V; Čada Z; Laštůvková J; Rašková D; Seeman P Clin Genet; 2020 Dec; 98(6):548-554. PubMed ID: 32860223 [TBL] [Abstract][Full Text] [Related]
3. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China. Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618 [TBL] [Abstract][Full Text] [Related]
4. Variant analysis of 92 Chinese Han families with hearing loss. Jin X; Huang S; An L; Zhang C; Dai P; Gao H; Ma X BMC Med Genomics; 2022 Jan; 15(1):12. PubMed ID: 35062939 [TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss. Xiang YB; Xu CY; Xu YZ; Li HZ; Zhou LL; Xu XQ; Chen ZH; Tang SH Mol Genet Genomic Med; 2020 Dec; 8(12):e1539. PubMed ID: 33095980 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations. Yu X; Lin Y; Xu J; Che T; Li L; Yang T; Wu H Orphanet J Rare Dis; 2020 Jan; 15(1):29. PubMed ID: 31992338 [TBL] [Abstract][Full Text] [Related]
8. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Sansović I; Meašić AM; Bobinec A; Morožin Pohovski L; Odak L; Vulin K; Lozić B; Kero M; Huljev Frković S; Pušeljić S Croat Med J; 2024 Jun; 65(3):198-208. PubMed ID: 38868966 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study. Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807 [TBL] [Abstract][Full Text] [Related]
11. [Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss]. Niu W; Xu H; Qin L; Wang G; Ding S; Xie C; Jia X; Liu H Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Feb; 35(2):131-136. PubMed ID: 33540994 [No Abstract] [Full Text] [Related]
12. Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing. Liu Y; Tan M; Cai L; Lv L; Chen Q; Chen W; Yang H; Xu Y Gene; 2022 Apr; 819():146258. PubMed ID: 35114279 [TBL] [Abstract][Full Text] [Related]
13. Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss. Guan J; Wang H; Lan L; Wu Y; Chen G; Zhao C; Wang D; Wang Q Mol Genet Genomic Med; 2020 Aug; 8(8):e1367. PubMed ID: 32567228 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing. Xiao C; Liu S; Wang H; Ding Y; Chen Y; Liu H Mol Genet Genomic Med; 2021 Apr; 9(4):e1634. PubMed ID: 33638616 [TBL] [Abstract][Full Text] [Related]
16. [Application of the real-time fluorescence PCR melting curve method in gene screening of non-syndromic hearing loss]. Liu YL; Jiang XH; Sun J; Mei LY; He CF; Deng YY; Wen J; Feng Y Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Apr; 54(4):286-291. PubMed ID: 30991779 [No Abstract] [Full Text] [Related]
17. 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]
18. [Analysis of genotypes on 850 newborns with Huang LH; Zhao XL; Cheng XH; Yu YD; Wen C; Li Y; Wang XL; Wang XY; Ruan Y; En H Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2023 Feb; 58(2):117-125. PubMed ID: 36748152 [No Abstract] [Full Text] [Related]
19. Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel. Ma J; Ma X; Lin K; Huang R; Bi X; Ming C; Li L; Li X; Li G; Zhao L; Yang T; Gao Y; Zhang T Hum Genomics; 2023 Jan; 17(1):1. PubMed ID: 36597107 [TBL] [Abstract][Full Text] [Related]
20. Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families. Pan J; Ma S; Teng Y; Liang D; Li Z; Wu L Clin Chim Acta; 2022 Jul; 532():53-60. PubMed ID: 35640668 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]