Is there a monosomy 10qter syndrome?

Clin Genet. 1982 Jan;21(1):33-5. doi: 10.1111/j.1399-0004.1982.tb02076.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, 6-12 and X*
  • Humans
  • Infant, Newborn
  • Male
  • Phenotype
  • Syndrome