Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)

J Med Genet. 2002 May;39(5):359-65. doi: 10.1136/jmg.39.5.359.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Chromosome Mapping
  • Female
  • Gene Deletion
  • Humans
  • Intellectual Disability / diagnosis*
  • Intellectual Disability / genetics*
  • Intellectual Disability / pathology
  • Male
  • Nephritis, Hereditary / diagnosis*
  • Nephritis, Hereditary / genetics*
  • Nephritis, Hereditary / pathology
  • Pedigree
  • X Chromosome* / ultrastructure

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