Dysmorphology

Pediatr Rev. 2019 Dec;40(12):609-618. doi: 10.1542/pir.2018-0331.
No abstract available

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Congenital Abnormalities / genetics*
  • Female
  • Genetic Diseases, Inborn* / genetics
  • Hamartoma Syndrome, Multiple / diagnosis
  • Hamartoma Syndrome, Multiple / genetics
  • Humans
  • Infant, Newborn
  • Loeys-Dietz Syndrome / diagnosis
  • Loeys-Dietz Syndrome / genetics
  • Male
  • Receptor, Transforming Growth Factor-beta Type II / genetics
  • Syndrome

Substances

  • Receptor, Transforming Growth Factor-beta Type II
  • TGFBR2 protein, human