Absence of NOTCH2 and Hey2 mutations in a familial alagille syndrome case with a novel frameshift mutation in JAG1

  • Inaam El-Rassy
  • , Jad Bou-Abdallah
  • , Sara Al-Ghadban
  • , Fadi Bitar
  • , Georges Nemer*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)937-939
Number of pages3
JournalAmerican Journal of Medical Genetics, Part A
Volume146
Issue number7
DOIs
Publication statusPublished - 1 Apr 2008
Externally publishedYes

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