Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda

This publication has 20 references indexed in Scilit:

• X-Linked Recessive Spondyloepiphyseal Dysplasia Tarda Clinical and Radiographic Evolution in a 6-Generation Kindred and Review of the Literature
  Medicine, 1999
• X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.
  Journal of Medical Genetics, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)
  Human Genetics, 1995
• The Gene for Spondyloepiphyseal Dysplasia (SEDL) Maps to Xp22 between DXS16 and DXS92
  Genomics, 1993
• Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome
  Human Genetics, 1988
• Spondylo-epiphyseal dysplasia tarda. The X-linked variety in three brothers
  The Journal of Bone and Joint Surgery. British volume, 1986
• The prevalence of skeletal dysplasias. An estimate of their minimum frequency and the number of patients requiring orthopaedic care
  The Journal of Bone and Joint Surgery. British volume, 1985
• Spondyloepiphyseal dysplasia tarda: a report of four cases in two families
  The British Journal of Radiology, 1973
• X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data.
  Journal of Medical Genetics, 1971