[Neonatal hypotonia in Prader-Willi syndrome due to t(15;16)]

Rev Neurol. 2000 Sep;31(5):499-500.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 15 / genetics*
  • Cytogenetics / methods
  • Female
  • Humans
  • Infant, Newborn
  • Muscle Hypotonia / etiology*
  • Prader-Willi Syndrome / complications*
  • Prader-Willi Syndrome / genetics*