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Q24672101-33AF313A-9C01-4EBD-ABEC-F5BEBC64B0BB
Q24672101-33AF313A-9C01-4EBD-ABEC-F5BEBC64B0BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-33AF313A-9C01-4EBD-ABEC-F5BEBC64B0BB
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
P2860
Q24672101-33AF313A-9C01-4EBD-ABEC-F5BEBC64B0BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-33AF313A-9C01-4EBD-ABEC-F5BEBC64B0BB
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wasDerivedFrom
aeb16120056258416028466f3fbfcc3d746e6e11
P2860
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.