Works matching AU Wang, Yupeng


Results: 280
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    Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling.

    Published in:
    Human Mutation, 2018, v. 39, n. 10, p. 1416, doi. 10.1002/humu.23590
    By:
    • Roessler, Erich;
    • Hu, Ping;
    • Marino, Juliana;
    • Hong, Sungkook;
    • Hart, Rachel;
    • Berger, Seth;
    • Martinez, Ariel;
    • Abe, Yu;
    • Kruszka, Paul;
    • Thomas, James W.;
    • Mullikin, James C.;
    • NISC Comparative Sequencing Program;
    • Wang, Yupeng;
    • Wong, Wendy S. W.;
    • Niederhuber, John E.;
    • Solomon, Benjamin D.;
    • Richieri‐Costa, Antônio;
    • Ribeiro‐Bicudo, L. A.;
    • Muenke, Maximilian
    Publication type:
    Article
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