Resultats de la cerca - Joshi Stephen

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  1. 1
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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 2018
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    Deficiency in the endocytic adaptor proteins PHETA1/2 impairs renal and craniofacial development per Kristin M. Ates, Tong Wang, Trevor Moreland, Rajalakshmi Veeranan-Karmegam, Manxiu Ma, Chelsi Jeter, Priya Anand, Wolfgang Wenzel, Hyung-Goo Kim, Lynne A. Wolfe, Joshi Stephen, David R. Adams, Thomas Markello, Cynthia J. Tifft, Robert Settlage, William A. Gahl, Graydon B. Gonsalvez, May Christine Malicdan, Heather Flanagan-Steet, Y. Albert Pan

    Publicat 2020
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