3q27.3 Microdeletion syndrome: further delineation of the second region of overlap and atopic dermatitis as a phenotypic feature

Clin Dysmorphol. 2017 Jul;26(3):154-156. doi: 10.1097/MCD.0000000000000177.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosome Disorders / diagnosis*
  • Chromosome Disorders / genetics*
  • Chromosomes, Human, Pair 3*
  • Comparative Genomic Hybridization
  • Dermatitis, Atopic / diagnosis*
  • Dermatitis, Atopic / genetics*
  • Genetic Association Studies
  • Humans
  • Karyotype
  • Male
  • Phenotype*
  • Syndrome