[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling]

Arch Pediatr. 1998 Aug;5(8):934-5. doi: 10.1016/s0929-693x(98)80208-x.
[Article in French]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Chromosomes, Human, Pair 15*
  • Chromosomes, Human, Pair 9*
  • Fatal Outcome
  • Female
  • Genetic Counseling*
  • Humans
  • Infant
  • Infant, Newborn
  • Karyotyping
  • Male
  • Prader-Willi Syndrome / diagnosis
  • Prader-Willi Syndrome / genetics*
  • Pregnancy
  • Prenatal Diagnosis
  • Translocation, Genetic / genetics*