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Jabs, EW
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created
[InstanceEdit:2029760] Rothfels, K, 2012-01-04
dbId
2029761
displayName
Jabs, EW
firstname
Ethylin W
initial
EW
publications
[LiteratureReference:2065827] Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
[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: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:2029809] Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
schemaClass
Person
surname
Jabs
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