Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.

مواد مشابهة

• Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.
  حسب: van den Elzen, M, وآخرون
  منشور في: (2014)
• Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1
  حسب: Van Den Elzen, M, وآخرون
  منشور في: (2014)
• The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males.
  حسب: Twigg, SR, وآخرون
  منشور في: (2006)
• Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome.
  حسب: Twigg, SR, وآخرون
  منشور في: (2004)
• Craniofrontonasal syndrome caused by introduction of a novel uATG in the 5′UTR of EFNB1
  حسب: Tavares, VL, وآخرون
  منشور في: (2018)