Second observation of Silver-Russel syndrome in a carrier of a reciprocal translocation with one breakpoint at site 17q25

Clin Genet. 1993 Jul;44(1):53-5. doi: 10.1111/j.1399-0004.1993.tb03845.x.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 17*
  • Dermatoglyphics
  • Facial Bones / abnormalities
  • Humans
  • Limb Deformities, Congenital
  • Male
  • Scoliosis / genetics
  • Syndrome
  • Translocation, Genetic*