Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

author
created [InstanceEdit:1637892] Rothfels, K, 2011-10-05
dbId 1637891
displayName Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
journal Oncogene
pages 7158-62
pubMedIdentifier 17525745
schemaClass LiteratureReference
title Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
url http://www.ncbi.nlm.nih.gov/pubmed/17525745
volume 26
year 2007

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