143 related articles for article (PubMed ID: 17661817)
1. Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree.
Meyer NC; Nishimura CJ; McMordie S; Smith RJ
Clin Genet; 2007 Aug; 72(2):130-7. PubMed ID: 17661817
[TBL] [Abstract][Full Text] [Related]
2. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
Alasti F; Sanati MH; Behrouzifard AH; Sadeghi A; de Brouwer AP; Kremer H; Smith RJ; Van Camp G
Int J Pediatr Otorhinolaryngol; 2008 Feb; 72(2):249-55. PubMed ID: 18022253
[TBL] [Abstract][Full Text] [Related]
3. Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.
Meyer NC; Alasti F; Nishimura CJ; Imanirad P; Kahrizi K; Riazalhosseini Y; Malekpour M; Kochakian N; Jamali P; Van Camp G; Smith RJ; Najmabadi H
Am J Med Genet A; 2007 Jul; 143A(14):1623-9. PubMed ID: 17431902
[TBL] [Abstract][Full Text] [Related]
4. An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.
Mustapha M; Weil D; Chardenoux S; Elias S; El-Zir E; Beckmann JS; Loiselet J; Petit C
Hum Mol Genet; 1999 Mar; 8(3):409-12. PubMed ID: 9949200
[TBL] [Abstract][Full Text] [Related]
5. A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.
Primignani P; Castorina P; Sironi F; Curcio C; Ambrosetti U; Coviello DA
Clin Genet; 2003 Jun; 63(6):516-21. PubMed ID: 12786758
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.
Batissoco AC; Abreu-Silva RS; Braga MC; Lezirovitz K; Della-Rosa V; Alfredo T; Otto PA; Mingroni-Netto RC
Ear Hear; 2009 Feb; 30(1):1-7. PubMed ID: 19125024
[TBL] [Abstract][Full Text] [Related]
7. Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss.
Iwasaki S; Harada D; Usami S; Nagura M; Takeshita T; Hoshino T
Arch Otolaryngol Head Neck Surg; 2002 Aug; 128(8):913-7. PubMed ID: 12162770
[TBL] [Abstract][Full Text] [Related]
8. Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes.
Balciuniene J; Dahl N; Jalonen P; Verhoeven K; Van Camp G; Borg E; Pettersson U; Jazin EE
Hum Genet; 1999 Sep; 105(3):211-6. PubMed ID: 10987647
[TBL] [Abstract][Full Text] [Related]
9. Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear.
de Heer AR; Pauw RJ; Huygen PL; Collin RW; Kremer H; Cremers CW
Audiol Neurootol; 2009; 14(3):153-62. PubMed ID: 19005249
[TBL] [Abstract][Full Text] [Related]
10. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A
Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572
[TBL] [Abstract][Full Text] [Related]
11. A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
Cryns K; Orzan E; Murgia A; Huygen PL; Moreno F; del Castillo I; Chamberlin GP; Azaiez H; Prasad S; Cucci RA; Leonardi E; Snoeckx RL; Govaerts PJ; Van de Heyning PH; Van de Heyning CM; Smith RJ; Van Camp G
J Med Genet; 2004 Mar; 41(3):147-54. PubMed ID: 14985372
[TBL] [Abstract][Full Text] [Related]
12. Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.
Hutchin T; Coy NN; Conlon H; Telford E; Bromelow K; Blaydon D; Taylor G; Coghill E; Brown S; Trembath R; Liu XZ; Bitner-Glindzicz M; Mueller R
Clin Genet; 2005 Dec; 68(6):506-12. PubMed ID: 16283880
[TBL] [Abstract][Full Text] [Related]
13. A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.
Bai H; Yang X; Temuribagen ; Guilan ; Suyalatu ; Narisu ; Wu H; Chen Y; Liu Y; Wu Q
BMC Med Genet; 2014 Mar; 15():34. PubMed ID: 25008054
[TBL] [Abstract][Full Text] [Related]
14. The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
Bazazzadegan N; Nikzat N; Fattahi Z; Nishimura C; Meyer N; Sahraian S; Jamali P; Babanejad M; Kashef A; Yazdan H; Sabbagh Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Reyhanifar F; Nouri N; Smith RJ; Kahrizi K; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2012 Aug; 76(8):1164-74. PubMed ID: 22695344
[TBL] [Abstract][Full Text] [Related]
15. Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report.
Sansović I; Meašić AM; Odak L; Kero M
Croat Med J; 2023 Oct; 64(5):329-333. PubMed ID: 37927186
[TBL] [Abstract][Full Text] [Related]
16. A novel TECTA mutation causes ARNSHL.
Asgharzade S; Tabatabaiefar MA; Modarressi MH; Ghahremani MH; Reiisi S; Tahmasebi P; Abdollahnejad F; Chaleshtori MH
Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():88-93. PubMed ID: 28012541
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.
Su Y; Tang WX; Gao X; Yu F; Dai ZY; Zhao JD; Lu Y; Ji F; Huang SS; Yuan YY; Han MY; Song YS; Zhu YH; Kang DY; Han DY; Dai P
PLoS One; 2014; 9(2):e89240. PubMed ID: 24586623
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.
Yamamoto N; Mutai H; Namba K; Morita N; Masuda S; Nishi Y; Nakano A; Masuda S; Fujioka M; Kaga K; Ogawa K; Matsunaga T
Orphanet J Rare Dis; 2017 Sep; 12(1):157. PubMed ID: 28946916
[TBL] [Abstract][Full Text] [Related]
19. Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer.
Collin RW; de Heer AM; Oostrik J; Pauw RJ; Plantinga RF; Huygen PL; Admiraal R; de Brouwer AP; Strom TM; Cremers CW; Kremer H
Eur J Hum Genet; 2008 Dec; 16(12):1430-6. PubMed ID: 18575463
[TBL] [Abstract][Full Text] [Related]
20. Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA.
Choi BY; Kim J; Chung J; Kim AR; Mun SJ; Kang SI; Lee SH; Kim N; Oh SH
PLoS One; 2014; 9(5):e97040. PubMed ID: 24816743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]