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

123 related items for PubMed ID: 32791904

  • 1. Delayed-Onset NOG Gene-Related Syndromic Conductive Deafness: A Case Report.
    Sun H, Qiao Y, Chen N, Yang H, Gao Z, Shang Y.
    Ear Nose Throat J; 2021 Jun; 100(3_suppl):333S-336S. PubMed ID: 32791904
    [Abstract] [Full Text] [Related]

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

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

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
    Ma C, Liu L, Wang FN, Tian HS, Luo Y, Yu R, Fan LL, Li YL.
    BMC Med Genet; 2019 Nov 06; 20(1):169. PubMed ID: 31694554
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Autosomal dominant stapes fixation, syndactyly, and symphalangism in a family with NOG mutation: Long term follow-up on surgical treatment.
    Westergaard-Nielsen M, Amstrup T, Wanscher JH, Brusgaard K, Ousager LB.
    Int J Pediatr Otorhinolaryngol; 2018 May 06; 108():208-212. PubMed ID: 29605356
    [Abstract] [Full Text] [Related]

  • 9. Involvement of the incudostapedial joint anomaly in conductive deafness.
    Suzuki M, Kanebayashi H, Kawano A, Hagiwara A, Furuse H, Yamaguchi T, Shimizu M.
    Acta Otolaryngol; 2008 May 06; 128(5):515-9. PubMed ID: 18421604
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Identification of an unknown frameshift variant of NOG in a Han Chinese family with proximal symphalangism.
    Yuan ZZ, Yu F, Jin JY, Jiao ZJ, Tang JY, Xiang R.
    Biosci Rep; 2020 Jun 26; 40(6):. PubMed ID: 32478388
    [Abstract] [Full Text] [Related]

  • 12. Multiple synostoses syndrome: Clinical report and retrospective analysis.
    Pan Z, Lu W, Li X, Huang S, Dai P, Yuan Y.
    Am J Med Genet A; 2020 Jun 26; 182(6):1438-1448. PubMed ID: 32259393
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Genetic and clinical phenotypic analysis of familial stapes sclerosis caused by an NOG mutation.
    Yu R, Jiang H, Liao H, Luo W.
    BMC Med Genomics; 2020 Dec 11; 13(1):187. PubMed ID: 33308208
    [Abstract] [Full Text] [Related]

  • 17. Unusual case of bilateral conductive deafness.
    Hoare TJ, Aldren CJ, Morgan DW, Bull TR.
    J Laryngol Otol; 1990 Jul 11; 104(7):560-1. PubMed ID: 2384713
    [Abstract] [Full Text] [Related]

  • 18. Stapes fixation accompanied with abnormal facial nerve pathway.
    Inagaki T, Kawano A, Ogawa Y, Shimizu M, Negishi M, Kawada Y, Suzuki M.
    Auris Nasus Larynx; 2014 Jun 11; 41(3):313-6. PubMed ID: 24581447
    [Abstract] [Full Text] [Related]

  • 19. Surgical findings and long-term hearing results in 3,050 stapedotomies for primary otosclerosis: a prospective study with the otology-neurotology database.
    Vincent R, Sperling NM, Oates J, Jindal M.
    Otol Neurotol; 2006 Dec 11; 27(8 Suppl 2):S25-47. PubMed ID: 16985478
    [Abstract] [Full Text] [Related]

  • 20. Hearing results of stapedotomy and malleo-vestibulopexy in congenital hearing loss.
    Kisilevsky VE, Bailie NA, Dutt SN, Halik JJ.
    Int J Pediatr Otorhinolaryngol; 2009 Dec 11; 73(12):1712-7. PubMed ID: 19800139
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.