Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 162

1.

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.

PMID:
10645953
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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 15;36(3):507-14.

PMID:
8884274
[PubMed - indexed for MEDLINE]
3.

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 21;84(2):145-50.

PMID:
10323740
[PubMed - indexed for MEDLINE]
4.

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.

PMID:
11781685
[PubMed - indexed for MEDLINE]
Free Article
5.

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.

PMID:
10445358
[PubMed - indexed for MEDLINE]
6.

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.

PMID:
10434119
[PubMed - indexed for MEDLINE]
7.

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 Jr, Witt PD, Mazaheri M, Diehl SR.

J Craniofac Genet Dev Biol. 1999 Jul-Sep;19(3):128-34.

PMID:
10589394
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
7825592
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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. Epub 2003 Aug 14.

PMID:
12920575
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
8069301
[PubMed - indexed for MEDLINE]
11.

Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.

Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC.

Hum Mutat. 2001 Nov;18(5):422-34.

PMID:
11668635
[PubMed - indexed for MEDLINE]
12.

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 22;547(1-2):49-53.

PMID:
15013698
[PubMed - indexed for MEDLINE]
13.

Phenotypic variability in van der Woude syndrome.

Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.

Genet Couns. 1995;6(3):221-6.

PMID:
8588850
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
10894430
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
10593995
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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. doi: 10.1097/SCS.0b013e3181edc528.

PMID:
20818247
[PubMed - indexed for MEDLINE]
17.

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 15;104(1):86-92.

PMID:
11746036
[PubMed - indexed for MEDLINE]
18.

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.

PMID:
10417286
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

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, et al.

Am J Hum Genet. 1990 Mar;46(3):486-91.

PMID:
2309700
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

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. doi: 10.1111/j.1834-7819.2009.01178.x.

PMID:
20415912
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk