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J T Prchal

Showing results (41-50 of 133) with videos related to

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Blood|September 1, 1987
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisT Coetzer, J Lawler, J T Prchal, et al.
The American Journal of Medicine|July 1, 1980
Urinary acidification in a patient with glucose-6-phosphate dehydrogenase deficiency. A reevaluation of the role of the hexose monophosphate shunt in renal acid secretionS G Rostand, R M Culpepper, J T Prchal
Gene|July 16, 1990
Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphismS H Yoon, C G Kentros, J T Prchal
American Journal of Human Genetics|November 1, 1982
Linkage studies in carriers of Lowe oculo-cerebro-renal syndromeH M Hittner, A J Carroll, J T Prchal
Science (New York, N.Y.)|June 30, 1995
Familial polycythemiaJ T Prchal, G L Semenza, J Prchal, et al.
The American Journal of Medicine|April 1, 1990
J. chain disease: a novel form of plasma cell dyscrasiaJ Mestecky, Z Moldoveanu, B A Julian, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1992
An acquired acute hepatic porphyria: a novel type of delta-aminolevulinate dehydratase inhibitionR Akagi, J T Prchal, C E Eberhart, et al.
The Journal of Biological Chemistry|May 5, 1991
Molecular defect of truncated beta-spectrin associated with hereditary elliptocytosis. Beta-spectrin GottingenS H Yoon, H Yu, S Eber, et al.
Proceedings 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.
Human Genetics|January 1, 1988
G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from LaosM C Poon, K Hall, C W Scott, et al.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
Blood|September 1, 1987
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisT Coetzer, J Lawler, J T Prchal, et al.
The American Journal of Medicine|July 1, 1980
Urinary acidification in a patient with glucose-6-phosphate dehydrogenase deficiency. A reevaluation of the role of the hexose monophosphate shunt in renal acid secretionS G Rostand, R M Culpepper, J T Prchal
Gene|July 16, 1990
Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphismS H Yoon, C G Kentros, J T Prchal
American Journal of Human Genetics|November 1, 1982
Linkage studies in carriers of Lowe oculo-cerebro-renal syndromeH M Hittner, A J Carroll, J T Prchal
Science (New York, N.Y.)|June 30, 1995
Familial polycythemiaJ T Prchal, G L Semenza, J Prchal, et al.
The American Journal of Medicine|April 1, 1990
J. chain disease: a novel form of plasma cell dyscrasiaJ Mestecky, Z Moldoveanu, B A Julian, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1992
An acquired acute hepatic porphyria: a novel type of delta-aminolevulinate dehydratase inhibitionR Akagi, J T Prchal, C E Eberhart, et al.
The Journal of Biological Chemistry|May 5, 1991
Molecular defect of truncated beta-spectrin associated with hereditary elliptocytosis. Beta-spectrin GottingenS H Yoon, H Yu, S Eber, et al.
Proceedings 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.
Human Genetics|January 1, 1988
G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from LaosM C Poon, K Hall, C W Scott, et al.
Pageof 14