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Journal Abstract Search

137 related items for PubMed ID: 16892395

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  • 2. Identification of a novel NOG mutation in a Chinese family with proximal symphalangism.
    Liu F, Huang Y, Liu L, Liang B, Qu Z, Huang G, Li C, Tian R, Jiang Z, Liu F, Yu X, Huang Y, Liu J, Tang Z.
    Clin Chim Acta; 2014 Feb 15; 429():129-33. PubMed ID: 24326127
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  • 6. 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 15; 82(6):514-20. PubMed ID: 22288654
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  • 9. Recurrent missense mutation of GDF5 (p.R438L) causes proximal symphalangism in a British family.
    Leonidou A, Irving M, Holden S, Katchburian M.
    World J Orthop; 2016 Dec 18; 7(12):839-842. PubMed ID: 28032038
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  • 10. Cushing proximal symphalangism and the NOG and GDF5 genes.
    Plett SK, Berdon WE, Cowles RA, Oklu R, Campbell JB.
    Pediatr Radiol; 2008 Feb 18; 38(2):209-15. PubMed ID: 17994231
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  • 11. Identification of a Novel NOG Missense Mutation in a Chinese Family With Symphalangism and Tarsal Coalitions.
    Xiong J, Tu W, Yan Y, Xiao K, Yao Y, Li S, Yang L, Zhou M, Liu Y, Hu J, Zhu F.
    Front Genet; 2019 Feb 18; 10():353. PubMed ID: 31105738
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  • 16. 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
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  • 17. Knock-in human GDF5 proregion L373R mutation as a mouse model for proximal symphalangism.
    Zhang X, Xing X, Liu X, Hu Y, Qu S, Wang H, Luo Y.
    Oncotarget; 2017 Dec 26; 8(69):113966-113976. PubMed ID: 29371961
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  • 18. GDF5 is a second locus for multiple-synostosis syndrome.
    Dawson K, Seeman P, Sebald E, King L, Edwards M, Williams J, Mundlos S, Krakow D.
    Am J Hum Genet; 2006 Apr 26; 78(4):708-12. PubMed ID: 16532400
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  • 19. Distal symphalangism: a report of two families.
    Poush JR.
    J Hered; 1991 Apr 26; 82(3):233-8. PubMed ID: 2061594
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