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

9 Citations (Scopus)
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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