FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing. - Meyers,G.A.; Day,D.; Goldberg,R.; Daentl,D.L.; Przylepa,K.A.; Abrams,L.J. (Am J Hum Genet, 1996)