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NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous... | ResearchHub
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NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway
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Authors
Ryan McDaniell
8 more
Ryan McDaniell
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David Piccoli
6 more
•
Nancy Spinner
Published
June 7, 2006
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Journal
The American Journal of Human Genetics
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Surgery
Show all topics
DOI
10.1086/505332
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publisher-specific-oa
Supporters
Support the authors with ResearchCoin
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Journal
The American Journal of Human Genetics
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Surgery
Show all topics
DOI
10.1086/505332
License
publisher-specific-oa
