Resultats de la cerca - K. P. Vinayan
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Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report per Joshi Stephen, Sheela Nampoothiri, K. P. Vinayan, Dhanya Yesodharan, Preetha Remesh, William A. Gahl, May Christine V. Malicdan
Publicat 2018Signatura: Carregant…Connect to this object online.
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