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XB--922911
Papers associated with kmt2a (and Disease Ontology)
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Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival., Griffin C, Coppenrath K, Khan D, Lin Z, Horb M, Saint-Jeannet JP., Dis Model Mech. March 1, 2025; 18 (3):  |
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A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB, Willsey HR, Xu Y, Xu Y, Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK, Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. August 17, 2021; 12 (11): 1094-1107.e6.  |
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