480 related articles for article (PubMed ID: 11781685)
1. 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]
2. Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.
Houdayer C; Soupre V; Rosenberg-Bourgin M; Martinez H; Tredano M; Feldmann D; Feingold J; Aymard P; Munnich A; Le Bouc Y; Vazquez MP; Bahuau M
Ann Genet; 1999; 42(2):69-74. PubMed ID: 10434119
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. [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]
8. 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]
9. 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]
10. Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.
Sander A; Murray JC; Scherpbier-Heddema T; Buetow KH; Weissenbach J; Zingg M; Ludwig K; Schmelzle R
Am J Hum Genet; 1995 Jan; 56(1):310-8. PubMed ID: 7825592
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Report of two cases with Van der Woude syndrome: a child and her mother.
Koçer U; Aksoy HM; Tiftikcioğlu YO; Cöloğlu H; Karaaslan O
Genet Couns; 2001; 12(4):341-6. PubMed ID: 11837602
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
