Now showing items 1-2 of 2

    • Pryweller, Jennifer Raechelle (2013-12-10)
      Department: Interdisciplinary Studies: Human Genetics
      Williams syndrome (WS) is a rare, neurodevelopmental disorder caused by the deletion of 26 genes on chromosome 7q11.23. WS has a well-defined auditory phenotype, characterized by a strong attraction and emotional reactivity ...
    • Broeckelmann, Eva Marie (2013-04-16)
      Department: Interdisciplinary Studies: Human Genetics
      A member of the TGF-â superfamily of cytokines, BMP2 not only plays a critical role in pattern formation and morphogenesis during early embryonic development, but also promotes osteoblast differentiation and bone formation, ...