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ASXL1mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures

Published in 2022 by Isabella Lin, Zain Awamleh, Angela Wei, Bianca Russell ORCID, Rosanna Weksberg, Valerie A. Arboleda ORCID
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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