CDKN1C mutations and genital anomalies

Am J Med Genet A. 2012 Jan;158A(1):265. doi: 10.1002/ajmg.a.34388. Epub 2011 Dec 2.
No abstract available

Publication types

  • Letter

MeSH terms

  • Beckwith-Wiedemann Syndrome / diagnosis
  • Beckwith-Wiedemann Syndrome / genetics*
  • Cyclin-Dependent Kinase Inhibitor p57 / genetics*
  • Genetic Association Studies
  • Genitalia / abnormalities*
  • Humans
  • Infant, Newborn
  • Male
  • Mutation
  • Sequence Analysis

Substances

  • CDKN1C protein, human
  • Cyclin-Dependent Kinase Inhibitor p57