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 *

166 related articles for article (PubMed ID: 22613756)

  • 21. 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]  

  • 22. Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3.
    Kooshavar D; Tabatabaiefar MA; Farrokhi E; Abolhasani M; Noori-Daloii MR; Hashemzadeh-Chaleshtori M
    Int J Pediatr Otorhinolaryngol; 2013 Feb; 77(2):189-93. PubMed ID: 23141803
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [The mutation 35delG of the gene of the connexin 26 is a frequent cause of autosomal-recessive non-syndromic hearing loss in Morocco].
    Ratbi I; Hajji S; Ouldim K; Aboussair N; Feldmann D; Sefiani A
    Arch Pediatr; 2007 May; 14(5):450-3. PubMed ID: 17229560
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.
    Haghighat-Nia A; Keivani A; Nadeali Z; Fazel-Najafabadi E; Hosseinzadeh M; Salehi M
    Int J Pediatr Otorhinolaryngol; 2015 Nov; 79(11):1892-5. PubMed ID: 26409293
    [TBL] [Abstract][Full Text] [Related]  

  • 25. GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort.
    Carlsson PI; Karltorp E; Carlsson-Hansén E; Åhlman H; Möller C; Vondöbeln U
    Acta Otolaryngol; 2012 Dec; 132(12):1301-5. PubMed ID: 23039283
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).
    Minárik G; Ferák V; Feráková E; Ficek A; Poláková H; Kádasi L
    Gen Physiol Biophys; 2003 Dec; 22(4):549-56. PubMed ID: 15113126
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cx26 gene mutations in idiopathic progressive hearing loss.
    Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
    J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).
    Mishra S; Pandey H; Srivastava P; Mandal K; Phadke SR
    Indian J Pediatr; 2018 Dec; 85(12):1061-1066. PubMed ID: 29542069
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Mutations of GJB2 gene in infants with non-syndromic hearing impairment].
    Shi GZ; Gong LX; Nie WY; Lin Q; Xiang LL; Xu XH; Qi YS
    Zhonghua Yi Xue Za Zhi; 2005 Mar; 85(10):689-92. PubMed ID: 15932734
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
    Cryns K; Orzan E; Murgia A; Huygen PL; Moreno F; del Castillo I; Chamberlin GP; Azaiez H; Prasad S; Cucci RA; Leonardi E; Snoeckx RL; Govaerts PJ; Van de Heyning PH; Van de Heyning CM; Smith RJ; Van Camp G
    J Med Genet; 2004 Mar; 41(3):147-54. PubMed ID: 14985372
    [TBL] [Abstract][Full Text] [Related]  

  • 32. GJB2 mutations in deaf population of Ilam (Western Iran): a different pattern of mutation distribution.
    Mahdieh N; Mahmoudi H; Ahmadzadeh S; Bakhtiyari S
    Eur Arch Otorhinolaryngol; 2016 May; 273(5):1161-5. PubMed ID: 26059209
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey.
    Tarkan Ö; Sari P; Demirhan O; Kiroğlu M; Tuncer Ü; Sürmelioğlu Ö; Ozdemir S; Yilmaz MB; Kara K
    J Laryngol Otol; 2013 Jan; 127(1):33-7. PubMed ID: 23171692
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
    Abidi O; Boulouiz R; Nahili H; Bakhouch K; Wakrim L; Rouba H; Chafik A; Hassar M; Barakat A
    Genet Test; 2008 Dec; 12(4):569-74. PubMed ID: 19072567
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
    Schade G; Kothe C; Ruge G; Hess M; Meyer CG
    Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular epidemiology of DFNB1 deafness in France.
    Roux AF; Pallares-Ruiz N; Vielle A; Faugère V; Templin C; Leprevost D; Artières F; Lina G; Molinari N; Blanchet P; Mondain M; Claustres M
    BMC Med Genet; 2004 Mar; 5():5. PubMed ID: 15070423
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients.
    Dalamón V; Béhèran A; Diamante F; Pallares N; Diamante V; Elgoyhen AB
    Hear Res; 2005 Sep; 207(1-2):43-9. PubMed ID: 15964725
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Low frequency of GJB2 mutations in thirty-five students with hearing loss in Chinese consanguineous families.
    Chen G; Fu S; Dong J; Chen P
    Int J Pediatr Otorhinolaryngol; 2011 Dec; 75(12):1535-7. PubMed ID: 21962949
    [TBL] [Abstract][Full Text] [Related]  

  • 39. GJB2-associated hearing loss undetected by hearing screening of newborns.
    Minami SB; Mutai H; Nakano A; Arimoto Y; Taiji H; Morimoto N; Sakata H; Adachi N; Masuda S; Sakamoto H; Yoshida H; Tanaka F; Morita N; Sugiuchi T; Kaga K; Matsunaga T
    Gene; 2013 Dec; 532(1):41-5. PubMed ID: 24013081
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].
    Li YH; Jiang H; Yang LJ; Xu HX; Li H; Li HW; Luo YH; Wang CW; Zou GH
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Aug; 45(8):645-51. PubMed ID: 21055240
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.