219 related articles for article (PubMed ID: 14757865)
21. Van der Woude Syndrome: IRF6 Mutations.
Sunny AP; Arunachal G; Danda S
Indian J Pediatr; 2019 Nov; 86(11):1070-1071. PubMed ID: 31468312
[No Abstract] [Full Text] [Related]
22. A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family With Van der Woude Syndrome.
Tan EC; Lim HW; Lim ECP; Lee ST
Cleft Palate Craniofac J; 2017 Jul; 54(4):442-445. PubMed ID: 27243668
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
26. 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]
27. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
Peyrard-Janvid M; Leslie EJ; Kousa YA; Smith TL; Dunnwald M; Magnusson M; Lentz BA; Unneberg P; Fransson I; Koillinen HK; Rautio J; Pegelow M; Karsten A; Basel-Vanagaite L; Gordon W; Andersen B; Svensson T; Murray JC; Cornell RA; Kere J; Schutte BC
Am J Hum Genet; 2014 Jan; 94(1):23-32. PubMed ID: 24360809
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Hemiscrotal agenesis with complete testicular descent in Van der Woude syndrome: a new phenotypic feature.
Eliezer DD; Goel H; Turner VM; Deshpande A
BMJ Case Rep; 2019 Sep; 12(9):. PubMed ID: 31488442
[TBL] [Abstract][Full Text] [Related]
30. [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]
31. 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]
32. Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
Rorick NK; Kinoshita A; Weirather JL; Peyrard-Janvid M; de Lima RL; Dunnwald M; Shanske AL; Moretti-Ferreira D; Koillinen H; Kere J; Mansilla MA; Murray JC; Goudy SL; Schutte BC
Am J Med Genet A; 2011 Jun; 155A(6):1314-21. PubMed ID: 21574244
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6.
Little HJ; Rorick NK; Su LI; Baldock C; Malhotra S; Jowitt T; Gakhar L; Subramanian R; Schutte BC; Dixon MJ; Shore P
Hum Mol Genet; 2009 Feb; 18(3):535-45. PubMed ID: 19036739
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Counseling dilemmas in EEC syndrome.
Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
[TBL] [Abstract][Full Text] [Related]
37. Interferon Regulatory Factor 6 Controls Proliferation of Keratinocytes From Children With Van der Woude Syndrome.
Hixon K; Rhea L; Standley J; Canady FJ; Canady JW; Dunnwald M
Cleft Palate Craniofac J; 2017 May; 54(3):281-286. PubMed ID: 27115562
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. 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]
[Previous] [Next] [New Search]