Microcephaly-cardiomyopathy syndrome: expansion of the phenotype

J Med Genet. 2003 Jun;40(6):e78. doi: 10.1136/jmg.40.6.e78.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Cardiomyopathies / diagnosis*
  • Cardiomyopathies / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • Microcephaly / diagnosis*
  • Microcephaly / genetics*
  • Phenotype*
  • Syndrome