Query author contributions in Reactome

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Details on Person Wilkie, AO

Class:Id	Person:1008205
_displayName	Wilkie, AO
_timestamp	2011-09-29 18:05:46
created	[InstanceEdit:1008204] Jupe, S, 2010-11-10
firstname	Andrew O M
initial	AO
modified	[InstanceEdit:1614762] Rothfels, K, 2011-09-29
surname	Wilkie
(author)	[LiteratureReference:1008233] A review of the molecular genetics of the human alpha-globin gene cluster [LiteratureReference:1637876] Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome [LiteratureReference:2029801] Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand [LiteratureReference:2029815] Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome [LiteratureReference:2032919] Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors [LiteratureReference:2033246] Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis [LiteratureReference:2071925] FGFs, their receptors, and human limb malformations: clinical and molecular correlations
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No pathways have been reviewed or authored by Wilkie, AO (1008205)