BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

539 related articles for article (PubMed ID: 8588850)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. Van der Woude syndrome with mental retardation: case report.
    Ugwu BT; Momoh JT
    East Afr Med J; 2001 Feb; 78(2):111-2. PubMed ID: 11682943
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.
    Sander A; Schmelzle R; Murray J
    Hum Mol Genet; 1994 Apr; 3(4):575-8. PubMed ID: 8069301
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32.
    Lees MM; Winter RM; Malcolm S; Saal HM; Chitty L
    J Med Genet; 1999 Dec; 36(12):888-92. PubMed ID: 10593995
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Van der Woude syndrome: clinical presentation in 64 patients.
    Huang JJ; Hou JW; Tan YC; Chen KT; Lo LJ; Chen YR
    Cleft Palate Craniofac J; 2007 Nov; 44(6):649-52. PubMed ID: 18177185
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and genetic features of Van der Woude syndrome in two large families in Brazil.
    Martelli-Junior H; Chaves MR; Swerts MS; de Miranda RT; Bonan PR; Coletta RD
    Cleft Palate Craniofac J; 2007 May; 44(3):239-43. PubMed ID: 17477759
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6.
    Busche A; Hehr U; Sieg P; Gillessen-Kaesbach G
    Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731
    [TBL] [Abstract][Full Text] [Related]  

  • 32. De novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic features.
    Salahshourifar I; Halim AS; Sulaiman WA; Ariffin R; Naili Muhamad Nor N; Zilfalil BA
    Cytogenet Genome Res; 2011; 134(2):83-7. PubMed ID: 21447942
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital.
    James O; Adeyemo WL; Emeka CI; Ogunlewe MO; Ladeinde AL; Butali A
    Afr J Paediatr Surg; 2014; 11(1):52-5. PubMed ID: 24647295
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic epidemiology and control of genetic expression in van der Woude syndrome.
    Burdick AB
    J Craniofac Genet Dev Biol Suppl; 1986; 2():99-105. PubMed ID: 3491128
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.
    Schutte BC; Bjork BC; Coppage KB; Malik MI; Gregory SG; Scott DJ; Brentzell LM; Watanabe Y; Dixon MJ; Murray JC
    Genome Res; 2000 Jan; 10(1):81-94. PubMed ID: 10645953
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks.
    Janku P; Robinow M; Kelly T; Bralley R; Baynes A; Edgerton MT
    Am J Med Genet; 1980; 5(2):117-23. PubMed ID: 7395906
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.
    Manjegowda DS; Prasad M; Veerappa AM; Ramachandra NB
    Genet Res (Camb); 2014 Oct; 96():e12. PubMed ID: 25579819
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and genetic studies of Van der Woude syndrome in Sweden.
    Wong FK; Karsten A; Larson O; Huggare J; Hagberg C; Larsson C; Teh BT; Linder-Aronson S
    Acta Odontol Scand; 1999 Apr; 57(2):72-6. PubMed ID: 10445358
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome.
    Miñones-Suárez L; Mas-Vidal A; Fernandez-Toral J; Llano-Rivas I; González-García M
    Pediatr Dermatol; 2012; 29(6):768-70. PubMed ID: 21995291
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 27.