Showing 1 - 1 results of 1 for search 'Linda R. Wang MD', query time: 0.03s Refine Results
  1. 1
    A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome

    A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome by Linda R. Wang MD, Aleksandar Radonjic BSc, Allison A. Dilliott BSc, Adam D. McIntyre BSc, Robert A. Hegele MD, FRCPC, FACP

    Published 2018
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: