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XB-ANAT-4079
Papers associated with roof of mouth (and wnt1)
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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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Sox9 function in craniofacial development and disease., Lee YH, Lee YH., Genesis. April 1, 2011; 49 (4): 200-8. |
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