Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

J Med Genet. 2005 Apr;42(4):328-35. doi: 10.1136/jmg.2004.028258.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 9 / genetics*
  • Craniofacial Abnormalities / genetics
  • Cytogenetics
  • Genotype*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Language Development Disorders
  • Microcephaly / genetics
  • Phenotype*
  • Syndrome