Phenotype of maternal UPD(14)

Am J Med Genet. 1996 Dec 2;66(1):89. doi: 10.1002/(SICI)1096-8628(19961202)66:1<89::AID-AJMG22>3.0.CO;2-L.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 14*
  • Female
  • Genomic Imprinting*
  • Humans
  • Male
  • Translocation, Genetic