Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome
TARTAGLIA, M, VALERI, S, VELARDI, F, DI ROCCO, C, BATTAGLIA, P. A
Published in Human genetics (01.05.1997)
Published in Human genetics (01.05.1997)
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