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

Samankaltaisia teoksia

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