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Novel truncating mutations in CTNND1 cause a dominant cra... | ResearchHub
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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
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Authors
Reham Alharatani
32 more
Reham Alharatani
•
Marie Hosey
30 more
•
Karen Liu
Published
July 27, 2019
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Preprint Server
Topics
Biology
Bioinformatics
Genetics And Genomics
Genetics
Craniofacial
Show all topics
DOI
10.1101/711184
License
cc-no
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Bioinformatics
Genetics And Genomics
Genetics
Craniofacial
Show all topics
DOI
10.1101/711184
License
cc-no
