BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

489 related articles for article (PubMed ID: 20415912)

  • 1. 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]  

  • 2. Genetic analysis in families with van der Woude syndrome.
    Burdick AB; Bixler D; Puckett CL
    J Craniofac Genet Dev Biol; 1985; 5(2):181-208. PubMed ID: 4019732
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Isolated lower lip fistulas in Van der Woude syndrome.
    Etöz OA; Etöz A
    J Craniofac Surg; 2009 Sep; 20(5):1612-4. PubMed ID: 19816310
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases].
    Kläusler M; Schinzel A; Gnoinski W; Hotz M; Perko M
    Schweiz Med Wochenschr; 1987 Jan; 117(4):127-34. PubMed ID: 3823824
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Phenotypic variability in van der Woude syndrome.
    Lacombe D; Pedespan JM; Fontan D; Chateil JF; Verloes A
    Genet Couns; 1995; 6(3):221-6. PubMed ID: 8588850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.
    Beiraghi S; Miller-Chisholm A; Kimberling WJ; Sun CE; Wang YF; Russell LJ; Khoshnevisan M; Storm AL; Long RE; Witt PD; Mazaheri M; Diehl SR
    J Craniofac Genet Dev Biol; 1999; 19(3):128-34. PubMed ID: 10589394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree.
    Moghe GA; Kaur MS; Thomas AM; Raseswari T; Swapna M; Rao L
    J Indian Soc Pedod Prev Dent; 2010; 28(2):104-9. PubMed ID: 20660977
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Van der Woude syndrome: a report of two cases.
    King NM; Cheong CH; Sanares AM
    J Clin Pediatr Dent; 2004; 28(3):267-71. PubMed ID: 15163158
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H; Wong FK; Rautio J; Ollikainen V; Karsten A; Larson O; Teh BT; Huggare J; Lahermo P; Larsson C; Kere J
    Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685
    [TBL] [Abstract][Full Text] [Related]  

  • 16. van der Woude syndrome in two families in China.
    Burdick AB; Ma LA; Dai ZH; Gao NN
    J Craniofac Genet Dev Biol; 1987; 7(4):413-8. PubMed ID: 3429616
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Correlations between microforms of the Van der Woude syndrome and cleft palate.
    Ranta R; Rintala AE
    Cleft Palate J; 1983 Apr; 20(2):158-62. PubMed ID: 6573981
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital lower lip pits (Van der Woude syndrome): report of a case.
    Kirzioglu Z; Ertürk MS
    J Contemp Dent Pract; 2006 Feb; 7(1):134-40. PubMed ID: 16491156
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 25.