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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2000 | 1 |
2003 | 1 |
2007 | 1 |
2013 | 1 |
2019 | 1 |
2024 | 0 |
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A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.
Neuron. 2000 Oct;28(1):273-85. doi: 10.1016/s0896-6273(00)00102-1.
Neuron. 2000.
PMID: 11087000
Free article.
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
Naz S, Alasti F, Mowjoodi A, Riazuddin S, Sanati MH, Friedman TB, Griffith AJ, Wilcox ER, Riazuddin S.
Naz S, et al.
J Med Genet. 2003 May;40(5):360-3. doi: 10.1136/jmg.40.5.360.
J Med Genet. 2003.
PMID: 12746400
Free PMC article.
No abstract available.
Item in Clipboard
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.
Meyer NC, et al.
Am J Med Genet A. 2007 Jul 15;143A(14):1623-9. doi: 10.1002/ajmg.a.31718.
Am J Med Genet A. 2007.
PMID: 17431902
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Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS.
Miyagawa M, Nishio SY, Ikeda T, Fukushima K, Usami S.
Miyagawa M, et al.
PLoS One. 2013 Oct 9;8(10):e75793. doi: 10.1371/journal.pone.0075793. eCollection 2013.
PLoS One. 2013.
PMID: 24130743
Free PMC article.
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Genetic testing for congenital non-syndromic sensorineural hearing loss.
Raymond M, Walker E, Dave I, Dedhia K.
Raymond M, et al.
Int J Pediatr Otorhinolaryngol. 2019 Sep;124:68-75. doi: 10.1016/j.ijporl.2019.05.038. Epub 2019 May 29.
Int J Pediatr Otorhinolaryngol. 2019.
PMID: 31163360
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