Phenotypic delineation of a 12q21 deletion syndrome

Clin Dysmorphol. 2019 Oct;28(4):198-201. doi: 10.1097/MCD.0000000000000274.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Alleles
  • Chromosome Deletion*
  • Chromosome Disorders / diagnosis*
  • Chromosome Disorders / genetics*
  • Chromosomes, Human, Pair 12*
  • Comparative Genomic Hybridization
  • Genetic Markers
  • Humans
  • Infant
  • Male
  • Phenotype*
  • Syndrome

Substances

  • Genetic Markers