Novel mutations in prenatal diagnosis of primary microcephaly

Prenat Diagn. 2006 Oct;26(10):989. doi: 10.1002/pd.1536.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Female
  • Genetic Linkage*
  • Homozygote
  • Humans
  • Microcephaly / diagnosis
  • Microcephaly / genetics*
  • Mutation
  • Nerve Tissue Proteins / genetics*
  • Pregnancy
  • Prenatal Diagnosis

Substances

  • ASPM protein, human
  • Nerve Tissue Proteins