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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.
Human Genetics|January 1, 1980
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in SardiniaU Testa, T Meloni, A Lania, et al.
Birth Defects Original Article Series|January 1, 1982
The pattern of thalassemia in NaplesG Pepe, L Lupi, A Mastrobuono, et al.
Clinical and Experimental Immunology|July 1, 1988
The establishment of cell lines from chronic B cell leukaemias: evidence of leukaemic origin by karyotypic abnormalities and Ig gene rearrangementJ V Melo, L Foroni, V Brito-Babapulle, et al.
Blood|December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangementsI Dokal, J Bungey, P Williamson, et al.
The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.
British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.
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