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XB--5824174
Papers associated with mtss1.2 (and Disease Ontology)
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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. |
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