769 related articles for article (PubMed ID: 17366841)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
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. 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]
9. Novel IRF6 mutations in Honduran Van der Woude syndrome patients.
Birkeland AC; Larrabee Y; Kent DT; Flores C; Su GH; Lee JH; Haddad J
Mol Med Rep; 2011; 4(2):237-41. PubMed ID: 21468557
[TBL] [Abstract][Full Text] [Related]
10. Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
Scioletti AP; Brancati F; Gatta V; Antonucci I; Peissel B; Pizzuti A; Mortellaro C; Tetè S; Gherlone E; Palka G; Stuppia L
J Craniofac Surg; 2010 Sep; 21(5):1654-6. PubMed ID: 20856073
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: review of the literature.
Salahshourifar I; Wan Sulaiman WA; Halim AS; Zilfalil BA
Eur J Med Genet; 2012 Jun; 55(6-7):389-93. PubMed ID: 22440537
[TBL] [Abstract][Full Text] [Related]
13. Lower lip pits in a patient with van der Woude syndrome.
Baghestani S; Sadeghi N; Yavarian M; Alghasi H
J Craniofac Surg; 2010 Sep; 21(5):1380-1. PubMed ID: 20818247
[TBL] [Abstract][Full Text] [Related]
14. The association between interferon regulatory factor 6 (IRF6) and nonsyndromic cleft lip with or without cleft palate in a Honduran population.
Diercks GR; Karnezis TT; Kent DT; Flores C; Su GH; Lee JH; Haddad J
Laryngoscope; 2009 Sep; 119(9):1759-64. PubMed ID: 19536891
[TBL] [Abstract][Full Text] [Related]
15. Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan.
Malik S; Kakar N; Hasnain S; Ahmad J; Wilcox ER; Naz S
Clin Genet; 2010 Sep; 78(3):247-56. PubMed ID: 20184620
[TBL] [Abstract][Full Text] [Related]
16. Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
Stanier P; Moore GE
Hum Mol Genet; 2004 Apr; 13 Spec No 1():R73-81. PubMed ID: 14722155
[TBL] [Abstract][Full Text] [Related]
17. Van der Woude syndrome: dentofacial features and implications for clinical practice.
Lam AK; David DJ; Townsend GC; Anderson PJ
Aust Dent J; 2010 Mar; 55(1):51-8. PubMed ID: 20415912
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Altered regulation of cell migration in IRF6-mutated orofacial cleft patients-derived primary cells reveals a novel role of Rho GTPases in cleft/lip palate development.
Ghassibe-Sabbagh M; El Hajj J; Al Saneh M; El Baba N; Abou Issa J; Al Haddad M; El Atat O; Sabbagh J; Abou Chebel N; El-Sibai M
Cells Dev; 2021 Jun; 166():203674. PubMed ID: 33994351
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
