Evidence for a single genetic locus in Clouston's hidrotic ectodermal dysplasia.

This publication has 6 references indexed in Scilit:

• Confirmation of Linkage of Clouston Syndrome (Hidrotic Ectodermal Dysplasia) to 13q11-q12.1 with Evidence for Multiple Independent Mutations
  Journal of Investigative Dermatology, 1998
• The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
  American Journal of Medical Genetics, 1997
• Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
  Nature, 1997
• Sequences and differential expression of three novel human type-II hair keratins
  Differentiation, 1997
• The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q
  Human Molecular Genetics, 1996
• Hidrotic Ectodermal Dysplasia
  Archives of Dermatology, 1977