[A case of Xp21 contiguous gene deletion syndrome: clinical and genetic study]

Zhonghua Er Ke Za Zhi. 2009 Oct;47(10):792-3.
[Article in Chinese]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Agenesis of Corpus Callosum*
  • Chromosomes, Human, X*
  • Gene Deletion*
  • Glycerol Kinase / genetics*
  • Humans
  • Infant
  • Male
  • Syndrome

Substances

  • Glycerol Kinase