Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly von ROESSLER, E, WARD, D. E, GAUDENZ, K, BELLONI, E, SCHERER, S. W, DONNAI, D, SIEGEL-BARTELT, J, TSUI, L.-C, MUENKE, M

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Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21 von Schell, Ute, Wienberg, Johannes, Köhler, Angelika, Bray-Ward, Patricia, Ward, Deeann E., Wilson, William G., Allen, William P., Lebel, Robert R., Sawyer, Jeffrey R., Campbell, Paul L., Aughton, David J., Punnett, Hope H., Lammer, Edward J., Kao, Fa-Ten, Ward, David C., Muenke, Maximilian

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A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22 von Feldman, George J., Ward, Deeann E., Lajeunie-Renier, Elisabeth, Saavedra, Dolores, Robin, Nathaniel H., Proud, Virginia, Robb, Laura J., Der Kaloustian, Vazken, Carey, John C., Cohen, M. Michael, Cormier, Valerie, Munnich, Arnold, Zackai, Elaine H., Wilkie, Andrew O. M., Arlen Price, R., Muenke, Maximilian

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