Search Results - Clegg, N J

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  1. 1
    Septopreoptic Holoprosencephaly: A Mild Subtype Associated with Midline Craniofacial Anomalies

    Septopreoptic Holoprosencephaly: A Mild Subtype Associated with Midline Craniofacial Anomalies by Hahn, J.S., Barnes, P.D., Clegg, N.J., Stashinko, E.E.

    Published 2010
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  2. 2
    A Cytogenetic and Genetic Characterization of a Group of Closely Linked Second Chromosome Mutations That Suppress Position-Effect Variegation in Drosophila Melanogaster

    A Cytogenetic and Genetic Characterization of a Group of Closely Linked Second Chromosome Mutations That Suppress Position-Effect Variegation in Drosophila Melanogaster by Sinclair, D. A., Ruddell, A. A., Brock, J. K., Clegg, N. J., Lloyd, V. K., Grigliatti, T. A.

    Published 1992
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  3. 3
    In vitro expansion of GGC:GCC repeats: identification of the preferred strand of expansion.

    In vitro expansion of GGC:GCC repeats: identification of the preferred strand of expansion. by Ji, J, Clegg, N J, Peterson, K R, Jackson, A L, Laird, C D, Loeb, L A

    Published 1996
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  4. 4
    A Cytogenetic Analysis of Chromosomal Region 31 of Drosophila Melanogaster

    A Cytogenetic Analysis of Chromosomal Region 31 of Drosophila Melanogaster by Clegg, N. J., Whitehead, I. P., Brock, J. K., Sinclair, D. A., Mottus, R., Stromotich, G., Harrington, M. J., Grigliatti, T. A.

    Published 1993
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  5. 5
    Enhancer of Polycomb is a suppressor of position-effect variegation in Drosophila melanogaster.

    Enhancer of Polycomb is a suppressor of position-effect variegation in Drosophila melanogaster. by Sinclair, D A, Clegg, N J, Antonchuk, J, Milne, T A, Stankunas, K, Ruse, C, Grigliatti, T A, Kassis, J A, Brock, H W

    Published 1998
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  6. 6
    TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype

    TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype by Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J, Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.

    Published 2011
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  7. 7
    Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function

    Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function by Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K, Domené, S, Vélez, J I, Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njølstad, P R, Brunner, H G, Carey, J C, Hehr, U, Müsebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R, Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B, Muenke, M

    Published 2009
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