Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (9) GO Terms (2) Nucleotides (126) Proteins (50) Interactants (41) Wiki
XB--5824174

Papers associated with mtss1.2 (and Disease Ontology)



???displayGene.coCitedPapers???
Show all mtss1.2 papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

Point mutations in human GLI3 cause Greig syndrome., Wild A, Kalff-Suske M, Vortkamp A, Bornholdt D, König R, Grzeschik KH., Hum Mol Genet. October 1, 1997; 6 (11): 1979-84.

???pagination.result.page??? 1