BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

50 related articles for article (PubMed ID: 18776652)

  • 1. 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]  

  • 2. Identification of homozygous mutations for hearing loss.
    Dianatpour M; Smith E; Hashemi SB; Farazifard MA; Nezafat N; Razban V; Mani A
    Gene; 2021 Apr; 778():145464. PubMed ID: 33524517
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations.
    Koohiyan M; Azadegan-Dehkordi F; Koohian F; Hashemzadeh-Chaleshtori M
    J Audiol Otol; 2019 Oct; 23(4):175-180. PubMed ID: 31569309
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics of hereditary hearing loss in east Iran population: A systematic review of
    Koohiyan M; Azadegan-Dehkordi F; Koohian F; Abolhasani M; Hashemzadeh-Chaleshtori M
    Intractable Rare Dis Res; 2019 Aug; 8(3):172-178. PubMed ID: 31523594
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
    Beheshtian M; Babanejad M; Azaiez H; Bazazzadegan N; Kolbe D; Sloan-Heggen C; Arzhangi S; Booth K; Mohseni M; Frees K; Azizi MH; Daneshi A; Farhadi M; Kahrizi K; Smith RJ; Najmabadi H
    Arch Iran Med; 2016 Oct; 19(10):720-728. PubMed ID: 27743438
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss.
    Masoudi M; Ahangari N; Poursadegh Zonouzi AA; Poursadegh Zonouzi A; Nejatizadeh A
    Iran J Public Health; 2016 May; 45(5):680-7. PubMed ID: 27398341
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
    Zeinali S; Davoudi-Dehaghani E; Azadmehr S; DabbaghBagheri S; Bagherian H; Jamali M; Zafarghandimotlagh F; Masoodifard M; BandehiSarhaddi A; Rejali L; Sahebi S
    Eur Arch Otorhinolaryngol; 2015 Sep; 272(9):2255-9. PubMed ID: 25012701
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Progress in understanding GJB2-linked deafness.
    Gualandi F; Martini A; Calzolari E
    Community Genet; 2003; 6(3):125-32. PubMed ID: 15237196
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review.
    Koohiyan M; Ahmadi A; Koohian F; Aghaei S; Amiri B; Hashemzadeh-Chaleshtori M
    Int J Pediatr Otorhinolaryngol; 2019 Apr; 119():136-140. PubMed ID: 30708180
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GJB2 mutations in Baluchi population.
    Naghavi A; Nishimura C; Kahrizi K; Riazalhosseini Y; Bazazzadegan N; Mohseni M; Smith RJ; Najmabadi H
    J Genet; 2008 Aug; 87(2):195-7. PubMed ID: 18776652
    [No Abstract]   [Full Text] [Related]  

  • 12. Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran.
    Naddafnia H; Noormohammadi Z; Irani S; Salahshoorifar I
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00780. PubMed ID: 31162818
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence of GJB2-associated deafness and outcomes of cochlear implantation in Iran.
    Daneshi A; Hassanzadeh S; Emamdjomeh H; Mohammadi SH; Arzhangi S; Farhadi M; Najmabadi H
    J Laryngol Otol; 2011 May; 125(5):455-9. PubMed ID: 21281533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.
    Wiszniewski W; Sobieszczanska-Radoszewska L; Nowakowska-Szyrwinska E; Obersztyn E; Bal J
    Genet Test; 2001; 5(2):147-8. PubMed ID: 11551103
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.