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Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay

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Mario Cat Free Get File - Colaboratory

Multi-input Drug-Controlled Switches of Mammalian Gene Expression Based on Engineered Nuclear Hormone Receptors

PDF) ZeroCostDL4Mic: an open platform to simplify access and use of Deep-Learning in Microscopy

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