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ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations

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Ibrahim,  Daniel
Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Ibrahim, D. (2014). ChIP-seq Reveals Mutation-Specific Pathomechanismus of HOXD13 Missense Mutations. PhD Thesis, Humboldt University, FB Mathemathik, Berlin.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0026-A32E-3
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