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.
118 related articles for article (PubMed ID: 37207672)
1. The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data. Xiang J; Peng J; Sun X; Lin Z; Li D; Ye H; Wang S; Bai Y; Wang X; Du P; Gao Y; Sun J; Pan S; Peng Z Clin Chem; 2023 Jul; 69(7):763-770. PubMed ID: 37207672 [TBL] [Abstract][Full Text] [Related]
2. Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients. Nishio SY; Usami SI Sci Rep; 2022 Jan; 12(1):634. PubMed ID: 35022556 [TBL] [Abstract][Full Text] [Related]
3. Frequency and clinical features of hearing loss caused by STRC deletions. Yokota Y; Moteki H; Nishio SY; Yamaguchi T; Wakui K; Kobayashi Y; Ohyama K; Miyazaki H; Matsuoka R; Abe S; Kumakawa K; Takahashi M; Sakaguchi H; Uehara N; Ishino T; Kosho T; Fukushima Y; Usami SI Sci Rep; 2019 Mar; 9(1):4408. PubMed ID: 30867468 [TBL] [Abstract][Full Text] [Related]
4. DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. Vona B; Hofrichter MA; Neuner C; Schröder J; Gehrig A; Hennermann JB; Kraus F; Shehata-Dieler W; Klopocki E; Nanda I; Haaf T Clin Genet; 2015; 87(1):49-55. PubMed ID: 26011646 [TBL] [Abstract][Full Text] [Related]
5. Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene. Čada Z; Šafka Brožková D; Balatková Z; Plevová P; Rašková D; Laštůvková J; Černý R; Bandúrová V; Koucký V; Hrubá S; Komarc M; Jenčík J; Poisson Marková S; Plzák J; Kluh J; Seeman P Eur Arch Otorhinolaryngol; 2019 Dec; 276(12):3353-3358. PubMed ID: 31552524 [TBL] [Abstract][Full Text] [Related]
6. Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization. Moteki H; Azaiez H; Sloan-Heggen CM; Booth K; Nishio SY; Wakui K; Yamaguchi T; Kolbe DL; Iwasa YI; Shearer AE; Fukushima Y; Smith RJ; Usami SI Ann Otol Rhinol Laryngol; 2016 Nov; 125(11):918-923. PubMed ID: 27469136 [TBL] [Abstract][Full Text] [Related]
8. Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach. Kim BJ; Oh DY; Han JH; Oh J; Kim MY; Park HR; Seok J; Cho SD; Lee SY; Kim Y; Carandang M; Kwon IS; Lee S; Jang JH; Choung YH; Lee S; Lee H; Hwang SM; Choi BY Genet Med; 2020 Jun; 22(6):1119-1128. PubMed ID: 32203226 [TBL] [Abstract][Full Text] [Related]
9. Utility of droplet digital PCR and NGS-based CNV clinical assays in hearing loss diagnostics: current status and future prospects. Rentas S; Abou Tayoun A Expert Rev Mol Diagn; 2021 Feb; 21(2):213-221. PubMed ID: 33554673 [No Abstract] [Full Text] [Related]
10. Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss. Sagong B; Baek JI; Bok J; Lee KY; Kim UK Int J Pediatr Otorhinolaryngol; 2016 Jan; 80():78-81. PubMed ID: 26746617 [TBL] [Abstract][Full Text] [Related]
11. Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus. Sack LM; Mertens L; Murphy E; Hutchinson L; Giersch ABS; Mason-Suares H Clin Chem; 2023 Jun; 69(6):583-594. PubMed ID: 37022747 [TBL] [Abstract][Full Text] [Related]
12. Rapid screening of copy number variations in Ito T; Kawashima Y; Fujikawa T; Honda K; Makabe A; Kitamura K; Tsutsumi T Hum Genome Var; 2019; 6():41. PubMed ID: 31645979 [TBL] [Abstract][Full Text] [Related]
13. STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Plevova P; Paprskarova M; Tvrda P; Turska P; Slavkovsky R; Mrazkova E Otol Neurotol; 2017 Dec; 38(10):e393-e400. PubMed ID: 28984810 [TBL] [Abstract][Full Text] [Related]
14. Novel Pathogenic Variants in the Gene Encoding Stereocilin ( Domínguez-Ruiz M; Ruiz-Palmero L; Buonfiglio PI; García-Vaquero I; Gómez-Rosas E; Goñi M; Villamar M; Morín M; Moreno-Pelayo MA; Elgoyhen AB; Del Castillo FJ; Dalamón V; Del Castillo I Biomedicines; 2023 Oct; 11(11):. PubMed ID: 38001944 [TBL] [Abstract][Full Text] [Related]
15. Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis. Han S; Zhang D; Guo Y; Fu Z; Guan G Front Genet; 2021; 12():707845. PubMed ID: 34621290 [No Abstract] [Full Text] [Related]
16. Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss. Simi A; Perry J; Schindler E; Oza A; Luo M; Hartman T; Krantz ID; Germiller JA; Kawai K; Kenna M Laryngoscope; 2021 Dec; 131(12):E2897-E2903. PubMed ID: 34111299 [TBL] [Abstract][Full Text] [Related]
17. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Francey LJ; Conlin LK; Kadesch HE; Clark D; Berrodin D; Sun Y; Glessner J; Hakonarson H; Jalas C; Landau C; Spinner NB; Kenna M; Sagi M; Rehm HL; Krantz ID Am J Med Genet A; 2012 Feb; 158A(2):298-308. PubMed ID: 22147502 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings. Abbasi W; French CE; Rockowitz S; Kenna MA; Eliot Shearer A Hum Genet; 2022 Apr; 141(3-4):387-400. PubMed ID: 34811589 [TBL] [Abstract][Full Text] [Related]
20. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents. Knijnenburg J; Oberstein SA; Frei K; Lucas T; Gijsbers AC; Ruivenkamp CA; Tanke HJ; Szuhai K J Med Genet; 2009 Jun; 46(6):412-7. PubMed ID: 19246478 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]