Papers associated with cranial muscle primordium (and mtss1.2)

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	MIM regulates vertebrate neural tube closure., Liu W., Development. May 1, 2011; 138 (10): 2035-47.
	Functional analysis of novel mutations in y(+)LAT-1 amino acid transporter gene causing lysinuric protein intolerance (LPI)., Mykkänen J., Hum Mol Genet. February 12, 2000; 9 (3): 431-8.
	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.
	Developmental potential., Holmgren RA., Genes Dev. February 1, 1992; 6 (2): 161-5.

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