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American Journal of Hematology|September 18, 2001
Genetic heterogeneity of primary familial and congenital polycythemiaR Kralovics, J T PrchalCurrent Opinion in Pediatrics|February 17, 2000
Congenital and inherited polycythemiaR Kralovics, J T PrchalBailliere'S Clinical Haematology|January 20, 2000
Haematopoietic progenitors and signal transduction in polycythaemia vera and primary thrombocythaemiaR Kralovics, J T PrchalThe Journal of Clinical Investigation|July 3, 1998
Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemiaR Kralovics, L Sokol, J T PrchalAmerican Journal of Hematology|March 8, 2000
A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assaysX T Gregg, R Kralovics, J T PrchalProceedings of the Association of American Physicians|December 12, 1997
The erythropoietin receptor gene is not linked with the polycythemia phenotype in a family with autosomal dominant primary polycythemiaR Kralovics, L Sokol, E H Broxson, et al.Blood|September 18, 1997
Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemiasR Kralovics, K Indrak, T Stopka, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2000
Development of a novel trans-lentiviral vector that affords predictable safetyX Wu, J K Wakefield, H Liu, et al.Pageof 12