Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

author
created [InstanceEdit:1637875] Rothfels, K, 2011年10月05日
dbId 1637876
displayName Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
journal Nat Genet
pages 165-72
pubMedIdentifier 7719344
schemaClass LiteratureReference
title Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
url http://www.ncbi.nlm.nih.gov/pubmed/7719344
volume 9
year 1995
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