Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1).

Por Park, J P, Moeschler, J B, Berg, S Z, Wurster-Hill, D H
Publicado em 1991

Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia.

Por Finkelstein, J E, Doege, K, Yamada, Y, Pyeritz, R E, Graham, J M, Moeschler, J B, Pauli, R M, Hecht, J T, Francomano, C A
Publicado em 1991

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.

Por Meyers, G. A., Day, D., Goldberg, R., Daentl, D. L., Przylepa, K. A., Abrams, L. J., Graham, J. M., Feingold, M., Moeschler, J. B., Rawnsley, E., Scott, A. F., Jabs, E. W.
Publicado em 1996