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XB-ANAT-493
Papers associated with mouth (and slc7a5)
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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921. |
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Spatial and temporal expression of the Grainyhead-like transcription factor family during murine development., Auden A., Gene Expr Patterns. October 1, 2006; 6 (8): 964-70. |
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Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality., Parrish M., Mol Cell Biol. August 1, 2004; 24 (16): 7102-12. |
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