Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation

Clin Genet. 2005 Apr;67(4):367-8. doi: 10.1111/j.1399-0004.2005.00417.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosomes, Human, X / genetics*
  • Female
  • Gene Deletion*
  • Humans
  • Ichthyosis, X-Linked / genetics*
  • Infant
  • Intellectual Disability / genetics*
  • Male
  • Nuclear Proteins / genetics*
  • Pedigree

Substances

  • Nuclear Proteins
  • VCX protein, human