BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 20461822)

  • 1. Highlighted article: "identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse" by Stottmann, Bjork, Doyle, and Beier.
    Genesis; 2010 May; 48(5):281. PubMed ID: 20461822
    [No Abstract]   [Full Text] [Related]  

  • 2. Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse.
    Stottmann RW; Bjork BC; Doyle JB; Beier DR
    Genesis; 2010 May; 48(5):303-8. PubMed ID: 20196077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Van-der-Woude Syndrome].
    Del Frari B; Amort M; Janecke AR; Schutte BC; Piza-Katzer H
    Klin Padiatr; 2008; 220(1):26-8. PubMed ID: 18095255
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gene symbol: IRF6. Disease: Van der Woude syndrome.
    Item CB; Turhani D; Thurnher D; Sinko K; Yerit K; Galev K; Wittwer G; Lanre Adeyemo W; Klemens F; Ewers R; Watzinger F
    Hum Genet; 2004 Jul; 115(2):175. PubMed ID: 15300989
    [No Abstract]   [Full Text] [Related]  

  • 5. Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
    Peyrard-Janvid M; Pegelow M; Koillinen H; Larsson C; Fransson I; Rautio J; Hukki J; Larson O; Karsten AL; Kere J
    Eur J Hum Genet; 2005 Dec; 13(12):1261-7. PubMed ID: 16160700
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
    Tan EC; Lim EC; Yap SH; Lee ST; Cheng J; Por YC; Yeow V
    Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.
    Brosch S; Baur M; Blin N; Reinert S; Pfister M
    Int J Mol Med; 2007 Jul; 20(1):85-9. PubMed ID: 17549393
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
    Ghassibé M; Bayet B; Revencu N; Verellen-Dumoulin C; Gillerot Y; Vanwijck R; Vikkula M
    Eur J Hum Genet; 2005 Nov; 13(11):1239-42. PubMed ID: 16132054
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
    Pegelow M; Peyrard-Janvid M; Zucchelli M; Fransson I; Larson O; Kere J; Larsson C; Karsten A
    Eur J Orthod; 2008 Apr; 30(2):169-75. PubMed ID: 18209213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome.
    Kim Y; Park JY; Lee TJ; Yoo HW
    Int J Mol Med; 2003 Oct; 12(4):465-8. PubMed ID: 12964020
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gene symbol: IRF6. Disease: Van der Woude syndrome.
    Mostowska A; Wójcicki P; Kobus K; Trzeciak WH
    Hum Genet; 2005 May; 116(6):534. PubMed ID: 15988826
    [No Abstract]   [Full Text] [Related]  

  • 12. Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.
    Ali A; Singh SK; Raman R
    Cleft Palate Craniofac J; 2009 Sep; 46(5):541-4. PubMed ID: 19929101
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.
    de Lima RL; Hoper SA; Ghassibe M; Cooper ME; Rorick NK; Kondo S; Katz L; Marazita ML; Compton J; Bale S; Hehr U; Dixon MJ; Daack-Hirsch S; Boute O; Bayet B; Revencu N; Verellen-Dumoulin C; Vikkula M; Richieri-Costa A; Moretti-Ferreira D; Murray JC; Schutte BC
    Genet Med; 2009 Apr; 11(4):241-7. PubMed ID: 19282774
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome.
    Gatta V; Scarciolla O; Cupaioli M; Palka C; Chiesa PL; Stuppia L
    Mutat Res; 2004 Mar; 547(1-2):49-53. PubMed ID: 15013698
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Orofacial clefting: update on the role of genetics.
    Ghassibe M; Bayet B; Revencu N; Desmyter L; Verellen-Dumoulin C; Gillerot Y; Deggouj N; Vanwijck R; Vikkula M;
    B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
    Item CB; Turhani D; Thurnher D; Yerit K; Sinko K; Wittwer G; Adeyemo WL; Frei K; Erginel-Unaltuna N; Watzinger F; Ewers R
    Int J Mol Med; 2005 Feb; 15(2):247-51. PubMed ID: 15647839
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The penetrance and variable expression of the Van der Woude syndrome: implications for genetic counseling.
    Shprintzen RJ; Goldberg RB; Sidoti EJ
    Cleft Palate J; 1980 Jan; 17(1):52-7. PubMed ID: 6928118
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome.
    Shotelersuk V; Srichomthong C; Yoshiura K; Niikawa N
    Int J Mol Med; 2003 Apr; 11(4):505-7. PubMed ID: 12632105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.
    Ben J; Jabs EW; Chong SS
    Gene Expr Patterns; 2005 Jun; 5(5):629-38. PubMed ID: 15939375
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.
    Koillinen H; Lahermo P; Rautio J; Hukki J; Peyrard-Janvid M; Kere J
    J Med Genet; 2005 Feb; 42(2):177-84. PubMed ID: 15689458
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.