Meyers, G. A., Day, D., Goldberg, R., Daentl, D. L., Przylepa, K. A., Abrams, L. J., . . . Jabs, E. W. (1996). 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.
استشهاد بنمط شيكاغوMeyers, G. A., et al. 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. 1996.
MLA استشهادMeyers, G. A., et al. 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. 1996.
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