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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

204 related items for PubMed ID: 15699718

  • 1. Teunissen-Cremers syndrome: a clinical, surgical, and genetic report.
    Weekamp HH, Kremer H, Hoefsloot LH, Kuijpers-Jagtman AM, Cruysberg JR, Cremers CW.
    Otol Neurotol; 2005 Jan; 26(1):38-51. PubMed ID: 15699718
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  • 2. Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis.
    Usami S, Abe S, Nishio S, Sakurai Y, Kojima H, Tono T, Suzuki N.
    Clin Genet; 2012 Dec; 82(6):514-20. PubMed ID: 22288654
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  • 3. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin.
    Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM.
    Am J Hum Genet; 2002 Sep; 71(3):618-24. PubMed ID: 12089654
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  • 4. P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes.
    Hirshoren N, Gross M, Banin E, Sosna J, Bargal R, Raas-Rothschild A.
    Eur J Med Genet; 2008 Sep; 51(4):351-7. PubMed ID: 18440889
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  • 12. Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing loss.
    Bayat A, Fijalkowski I, Andersen T, Abdulmunem SA, van den Ende J, Van Hul W.
    Am J Med Genet A; 2016 Jun; 170(6):1479-84. PubMed ID: 26994744
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  • 13. 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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