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 *

205 related articles for article (PubMed ID: 19371219)

  • 1. Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.
    Primignani P; Trotta L; Castorina P; Lalatta F; Sironi F; Radaelli C; Degiorgio D; Curcio C; Travi M; Ambrosetti U; Cesarani A; Garavelli L; Formigoni P; Milani D; Murri A; Cuda D; Coviello DA
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):209-17. PubMed ID: 19371219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.
    Utrera R; Ridaura V; Rodríguez Y; Rojas MJ; Mago L; Angeli S; Henríquez O
    Genet Test; 2007; 11(4):347-52. PubMed ID: 18294049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. GJB2 mutations and degree of hearing loss: a multicenter study.
    Snoeckx RL; Huygen PL; Feldmann D; Marlin S; Denoyelle F; Waligora J; Mueller-Malesinska M; Pollak A; Ploski R; Murgia A; Orzan E; Castorina P; Ambrosetti U; Nowakowska-Szyrwinska E; Bal J; Wiszniewski W; Janecke AR; Nekahm-Heis D; Seeman P; Bendova O; Kenna MA; Frangulov A; Rehm HL; Tekin M; Incesulu A; Dahl HH; du Sart D; Jenkins L; Lucas D; Bitner-Glindzicz M; Avraham KB; Brownstein Z; del Castillo I; Moreno F; Blin N; Pfister M; Sziklai I; Toth T; Kelley PM; Cohn ES; Van Maldergem L; Hilbert P; Roux AF; Mondain M; Hoefsloot LH; Cremers CW; Löppönen T; Löppönen H; Parving A; Gronskov K; Schrijver I; Roberson J; Gualandi F; Martini A; Lina-Granade G; Pallares-Ruiz N; Correia C; Fialho G; Cryns K; Hilgert N; Van de Heyning P; Nishimura CJ; Smith RJ; Van Camp G
    Am J Hum Genet; 2005 Dec; 77(6):945-57. PubMed ID: 16380907
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations.
    Santos RL; Aulchenko YS; Huygen PL; van der Donk KP; de Wijs IJ; Kemperman MH; Admiraal RJ; Kremer H; Hoefsloot LH; Cremers CW
    Int J Pediatr Otorhinolaryngol; 2005 Feb; 69(2):165-74. PubMed ID: 15656949
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GJB2 mutations in patients with nonsyndromic hearing loss from Croatia.
    Sansović I; Knezević J; Musani V; Seeman P; Barisić I; Pavelić J
    Genet Test Mol Biomarkers; 2009 Oct; 13(5):693-9. PubMed ID: 19814620
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L
    Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.
    Cordeiro-Silva Mde F; Barbosa A; Santiago M; Provetti M; Dettogni RS; Tovar TT; Rabbi-Bortolini E; Louro ID
    Mol Biol Rep; 2011 Feb; 38(2):1309-13. PubMed ID: 20563649
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Al-Achkar W; Al-Halabi B; Ali B; Moassass F
    Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.
    Marlin S; Feldmann D; Blons H; Loundon N; Rouillon I; Albert S; Chauvin P; Garabédian EN; Couderc R; Odent S; Joannard A; Schmerber S; Delobel B; Leman J; Journel H; Catros H; Lemarechal C; Dollfus H; Eliot MM; Delaunoy JL; David A; Calais C; Drouin-Garraud V; Obstoy MF; Goizet C; Duriez F; Fellmann F; Hélias J; Vigneron J; Montaut B; Matin-Coignard D; Faivre L; Baumann C; Lewin P; Petit C; Denoyelle F
    Arch Otolaryngol Head Neck Surg; 2005 Jun; 131(6):481-7. PubMed ID: 15967879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.
    Mahdieh N; Rabbani B; Shirkavand A; Bagherian H; Movahed ZS; Fouladi P; Rahiminejad F; Masoudifard M; Akbari MT; Zeinali S
    Genet Test Mol Biomarkers; 2011; 15(7-8):489-93. PubMed ID: 21388256
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.
    Esmaeili M; Bonyadi M; Nejadkazem M
    Int J Pediatr Otorhinolaryngol; 2007 Jun; 71(6):869-73. PubMed ID: 17368814
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.
    Mikstiene V; Jakaitiene A; Byckova J; Gradauskiene E; Preiksaitiene E; Burnyte B; Tumiene B; Matuleviciene A; Ambrozaityte L; Uktveryte I; Domarkiene I; Rancelis T; Cimbalistiene L; Lesinskas E; Kucinskas V; Utkus A
    BMC Genet; 2016 Feb; 17():45. PubMed ID: 26896187
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss.
    Evirgen N; Solak M; Dereköy S; Erdoğan M; Yildiz H; Eser B; Arikan S; Erkoç A
    Genet Test; 2008 Jun; 12(2):253-6. PubMed ID: 18554165
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.