BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

294 related articles for article (PubMed ID: 15656949)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.
    Beck C; Pérez-Álvarez JC; Sigruener A; Haubner F; Seidler T; Aslanidis C; Strutz J; Schmitz G
    Eur Arch Otorhinolaryngol; 2015 Oct; 272(10):2765-76. PubMed ID: 25214170
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.
    Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM
    Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Mutation analysis of GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city].
    Yuan Y; Huang D; Dai P; Zhu X; Yu F; Zhang X; Liu L; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2008 Jan; 22(1):14-7, 21. PubMed ID: 18338563
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods.
    Bartsch O; Vatter A; Zechner U; Kohlschmidt N; Wetzig C; Baumgart A; Nospes S; Haaf T; Keilmann A
    Audiol Neurootol; 2010; 15(6):375-82. PubMed ID: 20234132
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation in gap and tight junctions in patients with non-syndromic hearing loss.
    Belguith H; Tlili A; Dhouib H; Ben Rebeh I; Lahmar I; Charfeddine I; Driss N; Ghorbel A; Ayadi H; Masmoudi S
    Biochem Biophys Res Commun; 2009 Jul; 385(1):1-5. PubMed ID: 19254696
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both c.35delG of GJB2 and the 342-kb deletion involving GJB6.
    Bolz H; Schade G; Ehmer S; Kothe C; Hess M; Gal A
    Hear Res; 2004 Feb; 188(1-2):42-6. PubMed ID: 14759569
    [TBL] [Abstract][Full Text] [Related]  

  • 34. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R
    Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions.
    Bliznetz EA; Lalayants MR; Markova TG; Balanovsky OP; Balanovska EV; Skhalyakho RA; Pocheshkhova EA; Nikitina NV; Voronin SV; Kudryashova EK; Glotov OS; Polyakov AV
    J Hum Genet; 2017 Aug; 62(8):789-795. PubMed ID: 28405014
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele.
    Gualandi E; Ravani A; Berto A; Burdo S; Trevisi P; Ferlini A; Martini A; Calzolari E
    Acta Otolaryngol Suppl; 2004 May; (552):29-34. PubMed ID: 15219044
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 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. 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]  

    [Previous]   [Next]    [New Search]
    of 15.