Disorder of sex development in an infant with molecularly confirmed 46,XY, +der(10)t(10;21)(q21.1;q21.3), -21

Am J Med Genet A. 2014 Mar;164A(3):841-3. doi: 10.1002/ajmg.a.36354. Epub 2014 Jan 17.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 10*
  • Chromosomes, Human, Pair 21*
  • Comparative Genomic Hybridization
  • Disorders of Sex Development / diagnosis*
  • Disorders of Sex Development / genetics*
  • Fatal Outcome
  • Humans
  • Infant
  • Male
  • Phenotype
  • Translocation, Genetic*