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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

256 related items for PubMed ID: 18338563

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. GJB3/GJB6 screening in GJB2 carriers with idiopathic hearing loss: Is it necessary?
    Chen K, Wu X, Zong L, Jiang H.
    J Clin Lab Anal; 2018 Nov; 32(9):e22592. PubMed ID: 29926981
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. [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
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
    Yu X, Lin Y, Xu J, Che T, Li L, Yang T, Wu H.
    Orphanet J Rare Dis; 2020 Jan 28; 15(1):29. PubMed ID: 31992338
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
    Pandya A, Arnos KS, Xia XJ, Welch KO, Blanton SH, Friedman TB, Garcia Sanchez G, Liu MD XZ, Morell R, Nance WE.
    Genet Med; 2003 Jan 28; 5(4):295-303. PubMed ID: 12865758
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
    Xiang YB, Tang SH, Li HZ, Xu CY, Chen C, Xu YZ, Ding LR, Xu XQ.
    Int J Pediatr Otorhinolaryngol; 2019 Jul 28; 122():185-190. PubMed ID: 31035178
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 28; 272(10):2765-76. PubMed ID: 25214170
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 28; 72(11):1633-6. PubMed ID: 18809214
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.