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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 22903915)

  • 1. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran.
    Babanejad M; Fattahi Z; Bazazzadegan N; Nishimura C; Meyer N; Nikzat N; Sohrabi E; Najmabadi A; Jamali P; Habibi F; Smith RJ; Kahrizi K; Najmabadi H
    Am J Med Genet A; 2012 Oct; 158A(10):2485-92. PubMed ID: 22903915
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
    Davarnia B; Babanejad M; Fattahi Z; Nikzat N; Bazazzadegan N; Pirzade A; Farajollahi R; Nishimura C; Jalalvand K; Arzhangi S; Kahrizi K; Smith RJ; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):268-71. PubMed ID: 22172221
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
    Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Reiisi S; Pourreza MR; Noori-Daloii MR; Tabatabaiefar MA
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.
    Abbaspour Rodbaneh E; Panahi M; Rahimi B; Mokabber H; Farajollahi R; Davarnia B
    J Clin Lab Anal; 2021 Nov; 35(11):e24024. PubMed ID: 34581455
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.
    Azadegan-Dehkordi F; Ahmadi R; Koohiyan M; Hashemzadeh-Chaleshtori M
    Ann Hum Genet; 2019 Jan; 83(1):1-10. PubMed ID: 30175840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
    Bazazzadegan N; Sheffield AM; Sobhani M; Kahrizi K; Meyer NC; Van Camp G; Hilgert N; Abedini SS; Habibi F; Daneshi A; Nishimura C; Avenarius MR; Farhadi M; Smith RJ; Najmabadi H
    Am J Med Genet A; 2011 May; 155A(5):1202-11. PubMed ID: 21484990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA; Xie DH
    Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.
    Bonyadi MJ; Fotouhi N; Esmaeili M
    Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):637-40. PubMed ID: 24529908
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
    Hashemi SB; Ashraf MJ; Saboori M; Azarpira N; Darai M
    Mol Biol Rep; 2012 Dec; 39(12):10481-7. PubMed ID: 23073770
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Did the GJB2 35delG mutation originate in Iran?
    Norouzi V; Azizi H; Fattahi Z; Esteghamat F; Bazazzadegan N; Nishimura C; Nikzat N; Jalalvand K; Kahrizi K; Smith RJ; Najmabadi H
    Am J Med Genet A; 2011 Oct; 155A(10):2453-8. PubMed ID: 21910243
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
    Fattahi Z; Shearer AE; Babanejad M; Bazazzadegan N; Almadani SN; Nikzat N; Jalalvand K; Arzhangi S; Esteghamat F; Abtahi R; Azadeh B; Smith RJ; Kahrizi K; Najmabadi H
    Am J Med Genet A; 2012 Aug; 158A(8):1857-64. PubMed ID: 22736430
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.
    Kashef A; Nikzat N; Bazzazadegan N; Fattahi Z; Sabbagh-Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Najmabadi H; Kahrizi K
    Int J Pediatr Otorhinolaryngol; 2015 Feb; 79(2):136-8. PubMed ID: 25555641
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.
    Mahdieh N; Shirkavand A; Raeisi M; Akbari MT; Tekin M; Zeinali S
    Biochem Biophys Res Commun; 2010 Nov; 402(2):305-7. PubMed ID: 20937258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).
    Cohn ES; Kelley PM; Fowler TW; Gorga MP; Lefkowitz DM; Kuehn HJ; Schaefer GB; Gobar LS; Hahn FJ; Harris DJ; Kimberling WJ
    Pediatrics; 1999 Mar; 103(3):546-50. PubMed ID: 10049954
    [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. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
    Mehregan H; Mohseni M; Jalalvand K; Arzhangi S; Nikzat N; Banihashemi S; Kahrizi K; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():115-126. PubMed ID: 30579064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Screening of OTOF mutations in Iran: a novel mutation and review.
    Mahdieh N; Shirkavand A; Rabbani B; Tekin M; Akbari B; Akbari MT; Zeinali S
    Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1610-5. PubMed ID: 22906306
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal recessive nonsyndromic deafness genes: a review.
    Duman D; Tekin M
    Front Biosci (Landmark Ed); 2012 Jun; 17(6):2213-36. PubMed ID: 22652773
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.
    del Castillo I; Villamar M; Moreno-Pelayo MA; del Castillo FJ; Alvarez A; Tellería D; Menéndez I; Moreno F
    N Engl J Med; 2002 Jan; 346(4):243-9. PubMed ID: 11807148
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.