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XB-ANAT-14
Papers associated with diencephalon (and hoxb1)
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Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57. |
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XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010. |
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