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1938206
1938206
https://w3id.org/oc/corpus/br/1938206
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
P3181
65f500822c9b3e76933b31501d940b10600c9c8f
P3181
Q24540535-DD4B265F-4690-4B73-8795-690B28D0515F
P3181
1938206
https://w3id.org/oc/corpus/br/1938206