Showing 1 - 3 results of 3 for search 'Schwartz Charles E', query time: 0.03s Refine Results
  1. 1
    Absence of mutations in <it>NR2E1 </it>and <it>SNX3 </it>in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

    Absence of mutations in <it>NR2E1 </it>and <it>SNX3 </it>in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes by Simpson Elizabeth M, Schwartz Charles E, Slavotinek Anne, Morgan Chad T, Everman David B, Kumar Ravinesh A

    Published 2007
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  2. 2
    XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

    XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene by MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E

    Published 2005
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  3. 3
    Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C

    Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C by Grafodatskaya Daria, Chung Barian HY, Butcher Darci T, Turinsky Andrei L, Goodman Sarah J, Choufani Sana, Chen Yi-An, Lou Youliang, Zhao Chunhua, Rajendram Rageen, Abidi Fatima E, Skinner Cindy, Stavropoulos James, Bondy Carolyn A, Hamilton Jill, Wodak Shoshana, Scherer Stephen W, Schwartz Charles E, Weksberg Rosanna

    Published 2013
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