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Molecular Biology & Medicine|April 1, 1984
Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenaseD Toniolo, M G Persico, G Battistuzzi, et al.Proceedings of the National Academy of Sciences of the United States of America|April 29, 1999
Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individualsD J Araten, K Nafa, K Pakdeesuwan, et al.The Biochemical Journal|October 1, 1990
Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNAV Poggi, M Town, N S Foulkes, et al.The Journal of Investigative Dermatology|May 1, 1991
Analysis of beta, gamma, and delta T-cell receptor genes in lymphomatoid papulosis: cellular basis of two distinct histologic subsetsS Whittaker, N Smith, R R Jones, et al.Journal of Health Care for the Poor and Underserved|May 31, 2012
African American parents' HPV vaccination intent and concernsVetta L Sanders Thompson, Lauren D Arnold, Sheri R NotaroEthnicity & Disease|September 28, 2011
African American parents' attitudes toward HPV vaccinationVetta L Sanders Thompson, Lauren D Arnold, Sheri R NotaroHuman Molecular Genetics|June 1, 1992
Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotypeM Town, J M Bautista, P J Mason, et al.Acta Cytologica|March 1, 1996
Psammoma bodies and cells from in situ fallopian tube carcinoma in endometrial smears: a case reportR Luzzatto, G Sisson, L Luzzatto, et al.Acta Haematologica|January 1, 1976
Erythrocyte enzymes in neonatal juandiceU Bienzle, C E Effiong, V E Aimaku, et al.British Journal of Haematology|June 1, 1994
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.Pageof 21