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Summary Anatomy Item Literature (2282) Expression Attributions Wiki
XB-ANAT-1506

Papers associated with skeletal element (and arvcf)

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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.                  

ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus., Tran HT., Dev Dyn. December 1, 2011; 240 (12): 2680-7.                

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