Deletions of 9q21.3 including NTRK2 are associated with severe phenotype

Am J Med Genet A. 2015 Jan;167A(1):264-7. doi: 10.1002/ajmg.a.36797. Epub 2014 Oct 27.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 9*
  • Female
  • Humans