Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

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🔗 View Article (PMID 7874170)

Published in Nat Genet on November 01, 1994

Authors

E W Jabs1, X Li, A F Scott, G Meyers, W Chen, M Eccles, J I Mao, L R Charnas, C E Jackson, M Jaye

Author Affiliations

1: Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland 21287-3914.

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