158 related articles for article (PubMed ID: 10434119)
1. 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]
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. PubMed ID: 11781685
[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. 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; 36(3):507-14. PubMed ID: 8884274
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
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. 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]
12. 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]
13. 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]
14. Genetic linkage studies with cleft lip and palate: report of two family studies.
Spence MA; Glass L; Crandall BF; Stewart RE; Miles J; Falk RE; Field LL; Sparkes RS
J Craniofac Genet Dev Biol; 1983; 3(3):207-12. PubMed ID: 6580294
[TBL] [Abstract][Full Text] [Related]
15. [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases].
Kläusler M; Schinzel A; Gnoinski W; Hotz M; Perko M
Schweiz Med Wochenschr; 1987 Jan; 117(4):127-34. PubMed ID: 3823824
[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 in two families in China.
Burdick AB; Ma LA; Dai ZH; Gao NN
J Craniofac Genet Dev Biol; 1987; 7(4):413-8. PubMed ID: 3429616
[TBL] [Abstract][Full Text] [Related]
18. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
Zeiger JS; Hetmanski JB; Beaty TH; VanderKolk CA; Wyszynski DF; Bailey-Wilson JE; de Luna RO; Perandones C; Tolarova MM; Mosby T; Bennun R; Segovia M; Calda P; Pugh EW; Doheny K; McIntosh I
Eur J Hum Genet; 2003 Nov; 11(11):835-9. PubMed ID: 14571267
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 11668635
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]