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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 9220188

  • 21.
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  • 22. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.
    Takahashi T, Takahashi I, Komatsu M, Sawaishi Y, Higashi K, Nishimura G, Saito H, Takada G.
    Clin Genet; 2001 Dec; 60(6):447-51. PubMed ID: 11846737
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  • 25. Dominant symphalangism and conductive hearing loss.
    Makowski A, Latkowski B, Niebudek-Bogusz E.
    Rev Laryngol Otol Rhinol (Bord); 1995 Dec; 116(5):339-40. PubMed ID: 8677370
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  • 27. Stapes fixation associated with symphalangia.
    Ueda H, Miyazawa T, Fujimoto T, Yanagita N.
    Arch Otolaryngol Head Neck Surg; 1996 Oct; 122(10):1124-8. PubMed ID: 8859127
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  • 28. Complex facio-audio-symphalangism syndrome. An autosomal recessive type?
    Balci S, Yigitkanli I.
    Genet Couns; 2004 Oct; 15(4):463-8. PubMed ID: 15658623
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  • 30. Stapedectomy in Teunissen-Cremers Syndrome: Intraoperative Findings and Hearing Outcomes.
    Coombs AC, Bird PA.
    Otol Neurotol; 2016 Oct; 37(9):1332-4. PubMed ID: 27525709
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  • 34. 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
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  • 36. An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.
    Schmitt E, Gillenwater JY, Kelly TE.
    Am J Med Genet; 1982 Sep 11; 13(1):63-9. PubMed ID: 7137222
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  • 37. Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations.
    Thomeer HG, Admiraal RJ, Hoefsloot L, Kunst HP, Cremers CW.
    Otol Neurotol; 2011 Jun 11; 32(4):632-8. PubMed ID: 21358557
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  • 38.
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  • 39. Proximal symphalangism and congenital conductive hearing loss: otologic aspects.
    Ensink RJ, Sleeckx JP, Cremers CW.
    Am J Otol; 1999 May 11; 20(3):344-9. PubMed ID: 10337976
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