A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene

Hum Mol Genet. 1993 Jul;2(7):1073-4. doi: 10.1093/hmg/2.7.1073.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Base Sequence
  • DNA / genetics
  • Exons
  • Female
  • Growth Disorders / genetics*
  • Growth Hormone / deficiency*
  • Growth Hormone / genetics*
  • Heterozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Pedigree
  • Sequence Deletion*

Substances

  • Growth Hormone
  • DNA