FGFR2 and Pfeiffer syndrome: Andrew's identification of the Apert mutation in FGFR2 (Wilkie et al., 1995) immediately followed three related discoveries: FGFR2 mutations are also responsible for Crouzon, Jackson‐Weiss and Pfeiffer syndromes (Reardon et al., 1994; Jabs et al., 1994 and Muenke et al., 1994; Figure 7).