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Q35668685-AC88BA3D-251F-4603-A0AF-04063275223F
Q35668685-AC88BA3D-251F-4603-A0AF-04063275223F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35668685-AC88BA3D-251F-4603-A0AF-04063275223F
FGFR3 Deficiency Causes Multiple Chondroma-like Lesions by Upregulating Hedgehog Signaling.
P2860
Q35668685-AC88BA3D-251F-4603-A0AF-04063275223F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35668685-AC88BA3D-251F-4603-A0AF-04063275223F
rank
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Statement
wasDerivedFrom
28affe30e2c1b3d2de7a6921332250a7a20b50ec
P2860
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome