Additional EFNB1 Mutations in Craniofrontonasal Syndrome

Benzer Materyaller

• Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1
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• Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome()
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• Craniofrontonasal Syndrome Caused by Introduction of a Novel uATG in the 5′UTR of EFNB1
  Yazar:: Romanelli Tavares, Vanessa L., ve diğerleri
  Baskı/Yayın Bilgisi: (2019)