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Human Genetics|December 22, 1999
SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patientsL Yin, V Ferrand, M F Lavoué, et al.
American Journal of Human Genetics|January 23, 1999
Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneityR Dufourcq-Lagelouse, N Jabado, F Le Deist, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|March 12, 2008
Invasive aspergillosis and allogeneic hematopoietic stem cell transplantation in children: a 15-year experienceN Crassard, H Hadden, C Pondarré, et al.
Bone Marrow Transplantation|December 1, 1996
Juvenile myelomonocytic leukemia: analyses of treatment results in the EORTC Children's Leukemia Cooperative Group (CLCG)P Lutz, I Zix-Kieffer, G Souillet, et al.
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