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Results: 1 to 20 of 127

1.

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

Wong FK, Koillinen H, Rautio J, Teh BT, Ranta R, Karsten A, Larson O, Linder-Aronson S, Huggare J, Larsson C, Kere J.

J Med Genet. 2001 Mar;38(3):198-202. No abstract available.

PMID:
11303516
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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
3.

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
4.

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]
5.

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.

PMID:
10912714
[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.

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]
9.

Van der Woude syndrome and nonsyndromic cleft lip and palate.

Hecht JT, Wang Y, Blanton SH, Daiger SP.

Am J Hum Genet. 1992 Aug;51(2):442-4. No abstract available.

PMID:
1642245
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

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 Apr-Jun;28(2):104-9. doi: 10.4103/0970-4388.66749.

PMID:
20660977
[PubMed - indexed for MEDLINE]
Free Article
11.

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
12.

Linkage studies in a pedigree with Van der Woude syndrome.

Wienker TF, Hudek G, Bissbort S, Mayerová A, Mauff G, Bender K.

J Med Genet. 1987 Mar;24(3):160-2.

PMID:
3572998
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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. No abstract available.

PMID:
14757865
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

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]
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.

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.

PMID:
17122170
[PubMed - indexed for MEDLINE]
17.

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
18.

Van der Woude syndrome with mental retardation: case report.

Ugwu BT, Momoh JT.

East Afr Med J. 2001 Feb;78(2):111-2.

PMID:
11682943
[PubMed - indexed for MEDLINE]
19.

Clinical and genetic features of Van der Woude syndrome in two large families in Brazil.

Martelli-Junior H, Chaves MR, Swerts MS, de Miranda RT, Bonan PR, Coletta RD.

Cleft Palate Craniofac J. 2007 May;44(3):239-43.

PMID:
17477759
[PubMed - indexed for MEDLINE]
20.

Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India.

Field LL, Ray AK, Cooper ME, Goldstein T, Shaw DF, Marazita ML.

Am J Med Genet A. 2004 Oct 15;130A(3):265-71.

PMID:
15378549
[PubMed - indexed for MEDLINE]

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