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Human 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.Annals of Human Genetics|May 1, 1981
New genetic variants of glucose 6-phosphate dehydrogenase (G6PD) in ItalyG Sansone, L Perroni, U Testa, et al.Experimental Hematology|January 1, 1994
Retroviral-mediated gene transfer of a mutant H-ras gene into normal human bone marrow alters myeloid cell proliferation and differentiationJ Maher, F Colonna, D Baker, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.Cancer|October 1, 1991
Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.Annals of Human Genetics|October 1, 1989
A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.Pageof 20