A new case of proximal monosomy 1p36, extending the phenotype

Am J Med Genet A. 2008 Aug 1;146A(15):2018-22. doi: 10.1002/ajmg.a.32405.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 1*
  • Female
  • Humans
  • Infant
  • Karyotyping
  • Monosomy*
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Syndrome