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De novo nonsense mutations in ASXL1 cause Bohring-Opitz s... | ResearchHub
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De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
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Authors
Alexander Hoischen
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Alexander Hoischen
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Susanne Kjærgaard
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Bert Vries
Published
June 26, 2011
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Journal
Nature Genetics
Topics
Biology
Immunology
Genetics
Phenotype
Mutation
Show all topics
DOI
10.1038/ng.868
