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1377526
1377526
https://w3id.org/oc/corpus/br/1377526
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
P3181
6075b83ce1f334083ac8cceacf28d30a9d883dee
P3181
Q24672101-1CD6B209-D82F-4A32-8330-C884E4A3E3A5
P3181
1377526
https://w3id.org/oc/corpus/br/1377526