Query author contributions in Reactome

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Details on Person Jabs, EW

Class:Id	Person:2029761
_displayName	Jabs, EW
_timestamp	2012-01-04 22:02:47
created	[InstanceEdit:2029760] Rothfels, K, 2012-01-04
firstname	Ethylin W
initial	EW
surname	Jabs
(author)	[LiteratureReference:2029809] Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome [LiteratureReference:2032916] A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene [LiteratureReference:2060761] Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability [LiteratureReference:2060834] Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3 [LiteratureReference:2065827] Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
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No pathways have been reviewed or authored by Jabs, EW (2029761)