Showing 1 - 1 results of 1 for search 'Stefania Moia', query time: 0.01s Refine Results
  1. 1
    Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: a case report

    Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: a case report by Stefania Moia, Daniele Tessaris, Silvia Einaudi, Luisa de Sanctis, Gianni Bona, Simonetta Bellone, Flavia Prodam

    Published 2017
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: