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

This publication has 12 references indexed in Scilit:

• Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome
  Journal of Medical Genetics, 2001
• 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
  American Journal of Human Genetics, 1999
• Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
  American Journal of Medical Genetics, 1999
• Clinical and genetic studies of Van der Woude syndrome in Sweden
  Acta Odontologica Scandinavica, 1999
• Relationship between Lower-Lip Fistulae and Cleft Lip and/or Palate in Van der Woude Syndrome
  The Cleft Palate Craniofacial Journal, 1997
• 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
  Genomics, 1996
• Evidence for a microdeletion in 1q32–41 involving the gene responsible for Van der Woude syndrome
  Human Molecular Genetics, 1994
• Lip pits and deletion 1q32 → 41
  American Journal of Medical Genetics, 1987
• The Van der Woude syndrome (dominantly inherited lip pits and clefts).
  Journal of Medical Genetics, 1986
• Lower lip sinuses: I. Epidemiology, microforms and transverse sulci
  British Journal of Plastic Surgery, 1981