Inherited Xp21 deletion in a boy with complex glycerol kinase deficiency syndrome

Clin Genet. 1986 Jan;29(1):92-3. doi: 10.1111/j.1399-0004.1986.tb00777.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosome Deletion*
  • Female
  • Glycerol Kinase / deficiency*
  • Humans
  • Male
  • Ornithine Carbamoyltransferase Deficiency Disease
  • Phosphotransferases / deficiency*
  • Sex Chromosome Aberrations*
  • X Chromosome*

Substances

  • Phosphotransferases
  • Glycerol Kinase