181 related articles for article (PubMed ID: 10445358)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Novel mutations in the IRF6 gene for Van der Woude syndrome.
Wang X; Liu J; Zhang H; Xiao M; Li J; Yang C; Lin X; Wu Z; Hu L; Kong X
Hum Genet; 2003 Oct; 113(5):382-6. PubMed ID: 12920575
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.
Sander A; Moser H; Liechti-Gallati S; Grimm T; Zingg M; Raveh J
Hum Genet; 1993 Mar; 91(1):55-62. PubMed ID: 8454288
[TBL] [Abstract][Full Text] [Related]
10. Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).
Houdayer C; Bonaïti-Pellié C; Erguy C; Soupre V; Dondon MG; Bürglen L; Cougoureux E; Couderc R; Vazquez MP; Bahuau M
Am J Med Genet; 2001 Nov; 104(1):86-92. PubMed ID: 11746036
[TBL] [Abstract][Full Text] [Related]
11. Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.
Murray JC; Nishimura DY; Buetow KH; Ardinger HH; Spence MA; Sparkes RS; Falk RE; Falk PM; Gardner RJ; Harkness EM
Am J Hum Genet; 1990 Mar; 46(3):486-91. PubMed ID: 2309700
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.
Sertié AL; Sousa AV; Steman S; Pavanello RC; Passos-Bueno MR
Am J Hum Genet; 1999 Aug; 65(2):433-40. PubMed ID: 10417286
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
Schutte BC; Basart AM; Watanabe Y; Laffin JJ; Coppage K; Bjork BC; Daack-Hirsch S; Patil S; Dixon MJ; Murray JC
Am J Med Genet; 1999 May; 84(2):145-50. PubMed ID: 10323740
[TBL] [Abstract][Full Text] [Related]
16. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
