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The American Journal of Clinical Nutrition|May 1, 1981
Cataracts and riboflavin deficiencyH W Skalka, J T PrchalBlood|April 1, 1996
A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemiaM M Jenkins, J T PrchalArchives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1980
Presenile cataract formation and decreased activity of galactosemic enzymesH W Skalka, J T PrchalHuman Genetics|February 1, 1997
A high-frequency polymorphism of NADH-cytochrome b5 reductase in African-AmericansM M Jenkins, J T PrchalStem Cells (Dayton, Ohio)|May 1, 1993
Biogenesis of erythrocyte membrane skeleton in health and diseaseM Hanspal, J T Prchal, J PalekAmerican 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 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 PrchalInvestigative Ophthalmology & Visual Science|August 1, 1989
Presence of erythroid and nonerythroid spectrin transcripts in human lens and cerebellumS H Yoon, H Skalka, J T PrchalPageof 16