Associated Papers
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Supplement: NIHMS2125804-supplement-2.xlsx › TableS1A
Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.
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Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
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Biorxiv : the Preprint Server for Biology, 2025
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Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
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