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J T Prchal

Showing results (21-30 of 133) with videos related to

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Human Genetics|February 1, 1997
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-AmericansM M Jenkins, J T Prchal
Blood|January 1, 1994
Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiologyJ T Prchal, J F Prchal
Blood|July 1, 1995
Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosisE A Lowenthal, J T Prchal
Seminars in Hematology|January 1, 1997
Erythropoietin receptor mutations and human diseaseX T Gregg, J T Prchal
Stem Cells (Dayton, Ohio)|May 1, 1993
Biogenesis of erythrocyte membrane skeleton in health and diseaseM Hanspal, J T Prchal, J Palek
Lancet (London, England)|July 10, 1993
Primary familial and congenital polycythaemiaL Sokol, J Prchal, J T Prchal
American Journal of Human Genetics|June 1, 1988
RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in blacksA Yoshida, T Takizawa, J T Prchal
The 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 Prchal
American 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 Prchal
Human Genetics|March 1, 1995
A TaqI polymorphism in the human erythroid beta spectrin geneL Beeton, J T Prchal, T L Coetzer
Pageof 14

Showing results (21-30 of 133) with videos related to

Sort By:
Pageof 14
Human Genetics|February 1, 1997
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-AmericansM M Jenkins, J T Prchal
Blood|January 1, 1994
Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiologyJ T Prchal, J F Prchal
Blood|July 1, 1995
Parvovirus B19 induced red blood cell aplasia in a patient with hereditary pyropoikilocytosisE A Lowenthal, J T Prchal
Seminars in Hematology|January 1, 1997
Erythropoietin receptor mutations and human diseaseX T Gregg, J T Prchal
Stem Cells (Dayton, Ohio)|May 1, 1993
Biogenesis of erythrocyte membrane skeleton in health and diseaseM Hanspal, J T Prchal, J Palek
Lancet (London, England)|July 10, 1993
Primary familial and congenital polycythaemiaL Sokol, J Prchal, J T Prchal
American Journal of Human Genetics|June 1, 1988
RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in blacksA Yoshida, T Takizawa, J T Prchal
The 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 Prchal
American 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 Prchal
Human Genetics|March 1, 1995
A TaqI polymorphism in the human erythroid beta spectrin geneL Beeton, J T Prchal, T L Coetzer
Pageof 14