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 *

349 related articles for article (PubMed ID: 31731535)

  • 21. Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort.
    Cama E; Melchionda S; Palladino T; Carella M; Santarelli R; Genovese E; Benettazzo F; Zelante L; Arslan E
    Int J Audiol; 2009 Jan; 48(1):12-7. PubMed ID: 19173109
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.
    Minárik G; Tretinárová D; Szemes T; Kádasi L
    Int J Pediatr Otorhinolaryngol; 2012 Mar; 76(3):400-3. PubMed ID: 22281373
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The association between GJB2 mutation and GJB6 gene in non syndromic hearing loss school children.
    Asma A; Ashwaq A; Norzana AG; Atmadini AM; Ruszymah BH; Saim L; Wahida IF
    Med J Malaysia; 2011 Jun; 66(2):124-8. PubMed ID: 22106692
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing Impairment.
    Dadhich A; Bhargava S; Samdhani S; Malhotra B; Mathur P; Rawat A; Grover M
    Indian J Otolaryngol Head Neck Surg; 2023 Dec; 75(4):3575-3580. PubMed ID: 37974894
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Frequency of GJB2 and del(GJB6-D13S1830) mutations among an Ecuadorian mestizo population.
    Paz-y-Miño C; Beaty D; López-Cortés A; Proaño I
    Int J Pediatr Otorhinolaryngol; 2014 Oct; 78(10):1648-54. PubMed ID: 25085072
    [TBL] [Abstract][Full Text] [Related]  

  • 26. GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent.
    Shan J; Chobot-Rodd J; Castellanos R; Babcock M; Shanske A; Parikh SR; Morrow BE; Samanich J
    Int J Pediatr Otorhinolaryngol; 2010 Jun; 74(6):611-8. PubMed ID: 20381175
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions.
    Talbi S; Bonnet C; Boudjenah F; Mansouri MT; Petit C; Ammar Khodja F
    Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():157-160. PubMed ID: 31200317
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.
    Nahili H; Ridal M; Boulouiz R; Abidi O; Imken L; Rouba H; Alami MN; Chafik A; Hassar M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1633-6. PubMed ID: 18809214
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Allele-specific impairment of GJB2 expression by GJB6 deletion del(GJB6-D13S1854).
    Rodriguez-Paris J; Tamayo ML; Gelvez N; Schrijver I
    PLoS One; 2011; 6(6):e21665. PubMed ID: 21738759
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Absence of GJB6 mutations in Indian patients with non-syndromic hearing loss.
    Bhalla S; Sharma R; Khandelwal G; Panda NK; Khullar M
    Int J Pediatr Otorhinolaryngol; 2011 Mar; 75(3):356-9. PubMed ID: 21227513
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil.
    Esteves MC; de Lima Isaac M; Francisco AM; da Silva Junior WA; Ferreira CA; Dell'Aringa AH
    Eur Arch Otorhinolaryngol; 2014 Apr; 271(4):695-9. PubMed ID: 23553242
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Spectrum of
    Zheng BJ; Zhang T; Wang H; Tang XW; Zheng J; Lv JX; Guan MX
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Jun; 30(12):933-937. PubMed ID: 29771057
    [No Abstract]   [Full Text] [Related]  

  • 33. Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania.
    Rădulescu L; Mârţu C; Birkenhäger R; Cozma S; Ungureanu L; Laszig R
    Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):90-4. PubMed ID: 22070872
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Screening of GJB6 gene large deletions among Syrians with congenital hearing impairment.
    Zaidieh T; Habbal W; Monem F
    Genet Test Mol Biomarkers; 2015 Jul; 19(7):405-7. PubMed ID: 25989237
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
    Küçük Kurtulgan H; Altuntaş EE; Yıldırım ME; Özdemir Ö; Bağcı B; Sezgin İ
    J Int Adv Otol; 2019 Dec; 15(3):373-378. PubMed ID: 31846914
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program.
    Propst EJ; Stockley TL; Gordon KA; Harrison RV; Papsin BC
    Int J Pediatr Otorhinolaryngol; 2006 Mar; 70(3):435-44. PubMed ID: 16125251
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss.
    Chinetti V; Iossa S; Auletta G; Laria C; De Luca M; Di Leva F; Riccardi P; Giannini P; Gasparini P; Ciccodicola A; Marciano E; Franzè A
    Int J Audiol; 2010 Apr; 49(4):326-31. PubMed ID: 20233142
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.
    Kabahuma RI; Ouyang X; Du LL; Yan D; Hutchin T; Ramsay M; Penn C; Liu XZ
    Int J Pediatr Otorhinolaryngol; 2011 May; 75(5):611-7. PubMed ID: 21392827
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.