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Archives of Disease in Childhood|November 1, 1995
Infantile osteopetrosis; bone marrow transplantation from a cousin donorG M Taylor, S P Dearden, A M Will, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
Bone mineral density in childhood survivors of acute lymphoblastic leukemia treated without cranial irradiationBernadette M D Brennan, Zulf Mughal, Stephen A Roberts, et al.
Blood|April 18, 2009
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, et al.
Cell Reports|August 18, 2015
Deregulation of the Ras-Erk Signaling Axis Modulates the Enhancer LandscapeBehnam Nabet, Pilib Ó Broin, Jaime M Reyes, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|August 25, 2005
Efficacy of artesunate plus chloroquine for uncomplicated malaria in children in Sao Tome and Principe: a double-blind, randomized, controlled trialV S Gil, M C R Ferreira, F S M d'Alva, et al.
British Journal of Haematology|April 29, 2006
Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemiaStefan Meyer, Lisa M Barber, Daniel J White, et al.
The British Journal of Radiology|September 16, 2015
Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imagingStavros M Stivaros, Robert Alston, Neville B Wright, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcomeJulia L Clarke, Tom J Vulliamy, David Roper, et al.
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