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Allele Publication :

Type  Original Publication . Mgi Jnum  J:72517
Publication . Citation  Hajihosseini MK, et al. (2001) A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci U S A 98(7):3855-60

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