No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver-Russell syndrome cases

Clin Genet. 2003 Sep;64(3):252-4. doi: 10.1034/j.1399-0004.2003.00135.x.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Bone Diseases, Developmental / genetics*
  • Chromosomes, Human, Pair 7 / genetics*
  • Face / abnormalities
  • Female
  • Fetal Growth Retardation / genetics*
  • Genetic Markers
  • Head / abnormalities
  • Humans
  • Male
  • Phenotype
  • Sequence Deletion*
  • Syndrome
  • Uniparental Disomy*

Substances

  • Genetic Markers