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Summary Anatomy Item Literature (88) Expression Attributions Wiki
XB-ANAT-412

Papers associated with tooth (and tbx1)

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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.                  


Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene., Chieffo C., Genomics. August 1, 1997; 43 (3): 267-77.

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