Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)

Clin Dysmorphol. 2001 Apr;10(2):151-3. doi: 10.1097/00019605-200104000-00015.

Abstract

The molecular-cytogenetic characterization of a de novo pure partial trisomy 10(q24.33-qter) is described. This report provides information about the postnatal phenotype. The clinical findings observed in this case support the conclusion that the more severe disease related genes are located between 10q24.1 and q24.33.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosomes, Human, Pair 10*
  • Cytogenetics
  • Female
  • Humans
  • Infant
  • Phenotype
  • Trisomy*