Deletion of the App-Runx1 region in mice models human partial monosomy 21

Partial monosomy 21 (PM21) is a rare chromosomal abnormality that is characterized by the loss of a variable segment along human chromosome 21 (Hsa21). The clinical phenotypes of this loss are heterogeneous and range from mild alterations to lethal consequences, depending on the affected region of H...

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Main Authors: Thomas Arbogast (Author), Matthieu Raveau (Author), Claire Chevalier (Author), Valérie Nalesso (Author), Doulaye Dembele (Author), Hugues Jacobs (Author), Olivia Wendling (Author), Michel Roux (Author), Arnaud Duchon (Author), Yann Herault (Author)
Format: Book
Published: The Company of Biologists, 2015-06-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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