Search Results - Ward, Deeann

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  1. 1
    Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly

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

    Published in Human genetics
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  2. 2
    Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21

    Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21 by 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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  3. 3
    A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22

    A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22 by 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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  4. 4
    Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

    Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes by Yoshiura, Koh-ichiro, Leysens, Nancy J., Chang, Jenny, Ward, Deeann, Murray, Jeffrey C., Muenke, Maximilian

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  5. 5
    Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

    Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes by Yoshiura, Koh-ichiro, Leysens, Nancy J., Chang, Jenny, Ward, Deeann, Murray, Jeffrey C., Muenke, Maximilian

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