Terminal deletion of chromosome 10q26 due to a paternal translocation [(7;10)(q36;q26)]

Am J Med Genet. 1991 Dec 15;41(4):534-6. doi: 10.1002/ajmg.1320410434.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 10*
  • Chromosomes, Human, Pair 7
  • Female
  • Humans
  • Karyotyping
  • Male
  • Translocation, Genetic