BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 10445358)

  • 21. 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]  

  • 22. 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]  

  • 23. [Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases].
    Bozkurt M; Kapı E; Külahçı Y; Zor F; Benlier E; Balkan M; Kılınç N; Imirzalıoğlu N; Kuvat SV
    Kulak Burun Bogaz Ihtis Derg; 2010; 20(4):200-4. PubMed ID: 20626329
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Popliteal pterygium syndrome in a Swedish family--clinical findings and genetic analysis with the van der Woude syndrome locus at 1q32-q41.
    Wong FK; Gustafsson B
    Acta Odontol Scand; 2000 Apr; 58(2):85-8. PubMed ID: 10894430
    [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. 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]  

  • 27. Van der Woude Syndrome With a Novel Mutation in the IRF6 Gene.
    Ural A; Bilgen F; Çakmakli S; Bekerecioğlu M
    J Craniofac Surg; 2019 Jul; 30(5):e465-e467. PubMed ID: 31299817
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
    Schutte BC; Sander A; Malik M; Murray JC
    Genomics; 1996 Sep; 36(3):507-14. PubMed ID: 8884274
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entities.
    Houdayer C; Soupre V; Karcenty B; Vazquez MP; Odent S; Lacombe D; Le Bouc Y; Munnich A; Bahuau M
    Am J Med Genet; 2000 Mar; 91(2):161-3. PubMed ID: 10748420
    [No Abstract]   [Full Text] [Related]  

  • 30. A clinical and multi‑omics study of Van der Woude syndrome in three generations of a Chinese family.
    Yang K; Dong XY; Wu J; Zhu JJ; Tan Y; Yan YS; Lin L; Zhang DL
    Mol Med Rep; 2020 Oct; 22(4):2925-2931. PubMed ID: 32945398
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. 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]  

  • 34. [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]  

  • 35. A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.
    Matsuzawa N; Shimozato K; Natsume N; Niikawa N; Yoshiura K
    J Dent Res; 2006 Dec; 85(12):1143-6. PubMed ID: 17122170
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.
    Ghassibé M; Revencu N; Bayet B; Gillerot Y; Vanwijck R; Verellen-Dumoulin C; Vikkula M
    J Med Genet; 2004 Feb; 41(2):e15. PubMed ID: 14757865
    [No Abstract]   [Full Text] [Related]  

  • 37. [Clinical and genetic features of Chinese kindreds with Van der Woude syndrome caused by interferon regulatory factor 6 mutation].
    Du XY; Li XY; Wu B; Xie C; Tian WD
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2018 Dec; 36(6):623-627. PubMed ID: 30593107
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.
    Leslie EJ; Koboldt DC; Kang CJ; Ma L; Hecht JT; Wehby GL; Christensen K; Czeizel AE; Deleyiannis FW; Fulton RS; Wilson RK; Beaty TH; Schutte BC; Murray JC; Marazita ML
    Clin Genet; 2016 Jul; 90(1):28-34. PubMed ID: 26346622
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
    Pegelow M; Koillinen H; Magnusson M; Fransson I; Unneberg P; Kere J; Karsten A; Peyrard-Janvid M
    Cleft Palate Craniofac J; 2014 Jan; 51(1):49-55. PubMed ID: 23394314
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.