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 *

351 related articles for article (PubMed ID: 31992338)

  • 21. Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.
    Chen S; Dong C; Wang Q; Zhong Z; Qi Y; Ke X; Liu Y
    Genet Test Mol Biomarkers; 2016 Nov; 20(11):660-665. PubMed ID: 27610647
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
    Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P
    PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
    Riahi Z; Hammami H; Ouragini H; Messai H; Zainine R; Bouyacoub Y; Romdhane L; Essaid D; Kefi R; Rhimi M; Bedoui M; Dhaouadi A; Feldmann D; Jonard L; Besbes G; Abdelhak S
    Gene; 2013 Aug; 525(1):1-4. PubMed ID: 23680645
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. [Application of next generation sequencing in congenital sensorineural deafness].
    Xu B; Chen Y; Jiang A; Chen C; Wang K; Zheng J; Fu Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):811-815. PubMed ID: 29921047
    [No Abstract]   [Full Text] [Related]  

  • 30. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
    Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.
    Yuan Y; Yu F; Wang G; Huang S; Yu R; Zhang X; Huang D; Han D; Dai P
    J Transl Med; 2010 Dec; 8():127. PubMed ID: 21122151
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families.
    Chen G; Liu J; Dong J; Li J; Fu S
    Int J Pediatr Otorhinolaryngol; 2014 Feb; 78(2):244-7. PubMed ID: 24359977
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
    Pang X; Chai Y; Chen P; He L; Wang X; Wu H; Yang T
    Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1351-3. PubMed ID: 26100058
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China.
    Dai ZY; Sun BC; Huang SS; Yuan YY; Zhu YH; Su Y; Dai P
    Gene; 2015 Oct; 570(2):272-6. PubMed ID: 26095810
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals.
    Huang S; Huang B; Wang G; Yuan Y; Dai P
    PLoS One; 2015; 10(6):e0129662. PubMed ID: 26061099
    [TBL] [Abstract][Full Text] [Related]  

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