खोज परिणाम - Joshi Stephen
- प्रदर्शित 1 - 2 परिणाम 2
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1
Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report द्वारा Joshi Stephen, Sheela Nampoothiri, K. P. Vinayan, Dhanya Yesodharan, Preetha Remesh, William A. Gahl, May Christine V. Malicdan
प्रकाशित 2018बोधानक: लोड हो रहा है…Connect to this object online.
स्थित: लोड हो रहा है…
पुस्तक -
2
Deficiency in the endocytic adaptor proteins PHETA1/2 impairs renal and craniofacial development द्वारा 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
प्रकाशित 2020बोधानक: लोड हो रहा है…Connect to this object online.
स्थित: लोड हो रहा है…
पुस्तक