Reactome | Muenke, M

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created	[InstanceEdit:2023271] Rothfels, K, 2011-12-07
dbId	2023272
displayName	Muenke, M
firstname	Maximillian
initial	M
publications	[LiteratureReference:2023308] A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome [LiteratureReference:2045069] Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes [LiteratureReference:2033246] Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis
schemaClass	Person
surname	Muenke

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