Authors: Schmidt, N Van Dyke, DC Keppler-Noreuil, Z Muilenburg, A Patil, S Kanis, AB

Citation: N. Schmidt et al., Developmental delay and multiple congenital anomalies in a child with a unique combination of partial monosomy 18 and partial trisomy 16, DEVELOP MED, 43(2), 2001, pp. 130-132

Authors: Williams, JK Schutte, DL Holkup, PA Evers, C Muilenburg, A

Citation: Jk. Williams et al., Psychosocial impact of predictive testing for Huntington disease on support persons, AM J MED G, 96(3), 2000, pp. 353-359

Authors: Wu, YQ Nickerson, E Shaffer, LG Keppler-Noreuil, K Muilenburg, A

Citation: Yq. Wu et al., A case of Williams syndrome with a large, visible cytogenetic deletion, J MED GENET, 36(12), 1999, pp. 928-932