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Summary Anatomy Item Literature (57) Expression Attributions Wiki

Papers associated with cranial muscle primordium (and gli3)

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Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual., Sobetzko D., Am J Med Genet. January 31, 2000; 90 (3): 239-42.

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome., Kalff-Suske M., Hum Mol Genet. September 1, 1999; 8 (9): 1769-77.

Point mutations in human GLI3 cause Greig syndrome., Wild A., Hum Mol Genet. October 1, 1997; 6 (11): 1979-84.

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