Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34

[1]  J. Kere,et al.  Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome , 2001, Journal of medical genetics.

[2]  R. Winter,et al.  Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32 , 1999 .

[3]  M. Passos-Bueno,et al.  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. , 1999, American journal of human genetics.

[4]  W. Kimberling,et al.  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. , 1999, Journal of craniofacial genetics and developmental biology.

[5]  S. Patil,et al.  Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. , 1999, American journal of medical genetics.

[6]  R. Hammer,et al.  Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. , 1998, Development.

[7]  R. Taga,et al.  Relationship between Lower-Lip Fistulae and Cleft Lip and/or Palate in Van der Woude Syndrome , 1997 .

[8]  J. Murray,et al.  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. , 1996, Genomics.

[9]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[10]  E. Mariman,et al.  A Mutation in COL9A2 Causes Multiple Epiphyseal Dysplasia (EDM2) , 1996, Annals of the New York Academy of Sciences.

[11]  R. Schmelzle,et al.  Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome. , 1994, Human molecular genetics.

[12]  R. Winter,et al.  Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies. , 1993, Journal of medical genetics.

[13]  T. Eskes.  Congenital malformations worldwide: A report from the International Clearinghouse for Birth Defects Monitoring Systems , 1992 .

[14]  P. M. Falk,et al.  Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. , 1990, American journal of human genetics.

[15]  J. Opitz,et al.  Lip pits and deletion 1q32----41. , 1987, American journal of medical genetics.

[16]  A. Schinzel,et al.  [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases]. , 1987, Schweizerische medizinische Wochenschrift.

[17]  A. Schinzel,et al.  The Van der Woude syndrome (dominantly inherited lip pits and clefts). , 1986, Journal of medical genetics.

[18]  A. Vanderwoude.  Fistula labii inferioris congenita and its association with cleft lip and palate. , 1954 .

[19]  S. Gregory,et al.  A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. , 2000, Genome research.

[20]  A. Munnich,et al.  Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait. , 1999, Annales de genetique.

[21]  C. Larsson,et al.  Clinical and genetic studies of Van der Woude syndrome in Sweden. , 1999, Acta odontologica Scandinavica.

[22]  K. Christensen,et al.  Familial recurrence-pattern analysis of nonsyndromic isolated cleft palate--a Danish Registry study. , 1996, American journal of human genetics.

[23]  E. Mariman,et al.  A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2) , 1996, Nature Genetics.

[24]  J. Weissenbach,et al.  Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. , 1995, American journal of human genetics.

[25]  Burdick Ab.  Genetic epidemiology and control of genetic expression in van der Woude syndrome. , 1986 .

[26]  C. Puckett,et al.  Genetic analysis in families with van der Woude syndrome. , 1985, Journal of craniofacial genetics and developmental biology.

[27]  Walker Gf,et al.  Racial variation of cephalometric measurements in Hawaii. , 1982 .

[28]  R. Ranta,et al.  Lower lip sinuses: I. Epidemiology, microforms and transverse sulci. , 1981, British journal of plastic surgery.