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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 12210332)

  • 1. TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders.
    Splendore A; Passos-Bueno MR; Jabs EW; Van Maldergem L; Wulfsberg EA
    Am J Med Genet; 2002 Aug; 111(3):324-7. PubMed ID: 12210332
    [No Abstract]   [Full Text] [Related]  

  • 2. The branchial arch syndromes.
    Willshaw HE; Al-Ashkar F
    Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 3)():331-7. PubMed ID: 6585075
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Etiopathogentic aspects, clinical picture and differential diagnostic view of first and second branchial arch syndromes].
    Minervini G; Scioli F
    Arch Stomatol (Napoli); 1990; 31(3):611-22. PubMed ID: 2097978
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Syndromes of the 1st and 2nd branchial arch: pathogenesis and therapy. 1].
    Cordaro L; Cordaro M
    Dent Cadmos; 1987 Sep; 55(14):49-56, 59-60. PubMed ID: 3484268
    [No Abstract]   [Full Text] [Related]  

  • 5. High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes.
    Splendore A; Silva EO; Alonso LG; Richieri-Costa A; Alonso N; Rosa A; Carakushanky G; Cavalcanti DP; Brunoni D; Passos-Bueno MR
    Hum Mutat; 2000 Oct; 16(4):315-22. PubMed ID: 11013442
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Branchial arch syndromes.
    Alfi D; Lam D; Gateno J
    Atlas Oral Maxillofac Surg Clin North Am; 2014 Sep; 22(2):167-73. PubMed ID: 25171997
    [No Abstract]   [Full Text] [Related]  

  • 7. Macular degeneration associated with a novel Treacher Collins tcof1 mutation and evaluation of this mutation in age related macular degeneration.
    Goverdhan SV; Temple IK; Self J; Lotery AJ; Dixon MJ; Evans AR
    Br J Ophthalmol; 2005 Aug; 89(8):1063-4. PubMed ID: 16024866
    [No Abstract]   [Full Text] [Related]  

  • 8. Exclusion of TCOF1 mutations in a case of bilateral Goldenhar syndrome and one familial case of microtia with meatal atresia.
    Thiel CT; Rosanowski F; Kohlhase J; Reis A; Rauch A
    Clin Dysmorphol; 2005 Apr; 14(2):67-71. PubMed ID: 15770127
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature.
    Splendore A; Fanganiello RD; Masotti C; Morganti LS; Passos-Bueno MR
    Hum Mutat; 2005 May; 25(5):429-34. PubMed ID: 15832313
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Goldenhar's oculo-auricular dysplasia].
    Mohieddine M
    Bull Soc Ophtalmol Fr; 1980 Oct; 80(10):957-9. PubMed ID: 7449018
    [No Abstract]   [Full Text] [Related]  

  • 11. Mutations and new polymorphic changes in the TCOF1 gene of patients with oculo-auriculo-vertebral spectrum and Treacher-Collins syndrome.
    Su PH; Yu JS; Chen JY; Chen SJ; Li SY; Chen HN
    Clin Dysmorphol; 2007 Oct; 16(4):261-7. PubMed ID: 17786119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Malformative aspects involving the 1st branchial arch. Report of 3 cases].
    Caramia G; Massacesi L
    Minerva Med; 1972 Feb; 63(9):490-6. PubMed ID: 4622013
    [No Abstract]   [Full Text] [Related]  

  • 13. Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
    So RB; Gonzales B; Henning D; Dixon J; Dixon MJ; Valdez BC
    Gene; 2004 Mar; 328():49-57. PubMed ID: 15019983
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
    Teber OA; Gillessen-Kaesbach G; Fischer S; Böhringer S; Albrecht B; Albert A; Arslan-Kirchner M; Haan E; Hagedorn-Greiwe M; Hammans C; Henn W; Hinkel GK; König R; Kunstmann E; Kunze J; Neumann LM; Prott EC; Rauch A; Rott HD; Seidel H; Spranger S; Sprengel M; Zoll B; Lohmann DR; Wieczorek D
    Eur J Hum Genet; 2004 Nov; 12(11):879-90. PubMed ID: 15340364
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.
    Su PH; Chen JY; Chen SJ; Yu JS
    J Formos Med Assoc; 2006 Jun; 105(6):518-21. PubMed ID: 16801042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Participation of the conjunctiva in syndromes of the 1st and 2nd branchial arch].
    Kastrantas A; Kyrzopoulos D; Stamatinis C
    Bull Mem Soc Fr Ophtalmol; 1981; 93():162-8. PubMed ID: 7346087
    [No Abstract]   [Full Text] [Related]  

  • 17. Parental origin of mutations in sporadic cases of Treacher Collins syndrome.
    Splendore A; Jabs EW; Félix TM; Passos-Bueno MR
    Eur J Hum Genet; 2003 Sep; 11(9):718-22. PubMed ID: 12939661
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical features, treatment and genetic background of Treacher Collins syndrome.
    Marszałek B; Wójcicki P; Kobus K; Trzeciak WH
    J Appl Genet; 2002; 43(2):223-33. PubMed ID: 12080178
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.
    Zhang X; Fan Y; Zhang Y; Xue H; Chen X
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1410-5. PubMed ID: 23838542
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A functional SNP in the promoter region of TCOF1 is associated with reduced gene expression and YY1 DNA-protein interaction.
    Masotti C; Armelin-Correa LM; Splendore A; Lin CJ; Barbosa A; Sogayar MC; Passos-Bueno MR
    Gene; 2005 Oct; 359():44-52. PubMed ID: 16102917
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.