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Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene
D Steinberger1, J B Mulliken, U Müller
1Institut für Humangenetik, Justus-Liebig-Universität, Giessen, Germany.
Human Mutation
|January 1, 1996
Abstract
No abstract available in PubMed .
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