BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 26211601)

  • 1. Novel NOG mutation in Japanese patients with stapes ankylosis with broad thumbs and toes.
    Ishino T; Takeno S; Hirakawa K
    Eur J Med Genet; 2015 Sep; 58(9):427-32. PubMed ID: 26211601
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.
    Ganaha A; Kaname T; Akazawa Y; Higa T; Shinjou A; Naritomi K; Suzuki M
    J Hum Genet; 2015 Jan; 60(1):27-34. PubMed ID: 25391606
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 182(6):1438-1448. PubMed ID: 32259393
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A comprehensive review of reported heritable noggin-associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term: NOG-related-symphalangism spectrum disorder (NOG-SSD).
    Potti TA; Petty EM; Lesperance MM
    Hum Mutat; 2011 Aug; 32(8):877-86. PubMed ID: 21538686
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. 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
    [TBL] [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; 108():208-212. PubMed ID: 29605356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 13(1):187. PubMed ID: 33308208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tarsal-carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation.
    Das Bhowmik A; Salem Ramakumaran V; Dalal A
    Am J Med Genet A; 2018 Jan; 176(1):219-224. PubMed ID: 29159868
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variable phenotypes of multiple synostosis syndrome in patients with novel NOG mutations.
    Lee BH; Kim OH; Yoon HK; Kim JM; Park K; Yoo HW
    Joint Bone Spine; 2014 Dec; 81(6):533-6. PubMed ID: 25241334
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Is the Conductive Hearing Loss in NOG-Related Symphalangism Spectrum Disorder Congenital?
    Nakashima T; Ganaha A; Tsumagari S; Nakamura T; Yamada Y; Nakamura E; Usami SI; Tono T
    ORL J Otorhinolaryngol Relat Spec; 2021; 83(3):196-202. PubMed ID: 33588412
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 51(4):351-7. PubMed ID: 18440889
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability.
    Pang X; Luo H; Chai Y; Wang X; Sun L; He L; Chen P; Wu H; Yang T
    PLoS One; 2015; 10(3):e0120816. PubMed ID: 25815513
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder.
    Takano K; Ogasawara N; Matsunaga T; Mutai H; Sakurai A; Ishikawa A; Himi T
    Hum Genome Var; 2016; 3():16023. PubMed ID: 27508084
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder.
    Carlson RJ; Quesnel A; Wells D; Brownstein Z; Gilony D; Gulsuner S; Leppig KA; Avraham KB; King MC; Walsh T; Rubinstein J
    Otol Neurotol; 2021 Sep; 42(8):e1143-e1151. PubMed ID: 34049328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Tarsal-carpal coalition syndrome: a familial case].
    Caino S; Dello Ruso B; Fano V; Obregón MG
    An Pediatr (Barc); 2012 Jun; 76(6):355-9. PubMed ID: 22326510
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Proximal symphalangism and premature ovarian failure.
    Kadi N; Tahiri L; Maziane M; Mernissi FZ; Harzy T
    Joint Bone Spine; 2012 Jan; 79(1):83-4. PubMed ID: 22088931
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical observation and genetic analysis of a SYNS1 family caused by novel NOG gene mutation.
    Zhang Z; Lu Y; Cao JY; Wang L; Li LK; Wang C; Ye X; Ji YM; Tu LY; Sun Y
    Mol Genet Genomic Med; 2022 May; 10(5):e1933. PubMed ID: 35332702
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.