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<http://identifiers.org/pubmed/16380922> <http://purl.org/dc/terms/title> "Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation." <http://purl.org/np/RAUuQX3Pn_kg02dLIbaHrRqtv8p-LqsAkDYvftNOpzzRg#provenance> .
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