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Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome.
M Tartaglia, S Valeri, F Velardi, C Di Rocco, P A Battaglia
Human Genetics 1997; 99(5):602-606
ICID: 841264
IC™ Value: 6.00
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