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Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variantsL Dente, M D'Urso, S Di Maio, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1979
Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type-A-) is expressed in the liverO A Oluboyede, G J Esan, T I Francis, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.
Haematologica|March 1, 1997
Small bowel infarction by AspergillusL Catalano, M Picardi, D Anzivino, et al.
Genomics|April 10, 1995
Genomic structure and sequence of the Fugu rubripes glucose-6-phosphate dehydrogenase gene (G6PD)P J Mason, D J Stevens, L Luzzatto, et al.
Human Heredity|May 1, 1996
Molecular characterization of G6PD deficiency in OmanS Daar, T J Vulliamy, J Kaeda, et al.
Tumori|August 31, 1989
Risk factors for soft tissue sarcomas in childhood: a case-control studyC Magnani, G Pastore, L Luzzatto, et al.
Somatic Cell Genetics|July 1, 1983
Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybridsM D'Urso, C Mareni, D Toniolo, et al.
American Journal of Human Genetics|January 1, 1977
Comparison of GdA and GdB activities in Nigerians. A study of the variation of the G6PD activityG Battistuzzi, G J Esan, F A Fasuan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.
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