A case which further refines the critical region for 15q25.2 microduplication phenotypes

Acta Neurol Belg. 2016 Dec;116(4):683-685. doi: 10.1007/s13760-016-0620-7. Epub 2016 Feb 29.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosomes, Human, Pair 15 / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Phenotype
  • Segmental Duplications, Genomic / genetics*