Search Results - Stefania Moia

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    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
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