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Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this siteP Szabo, M Purrello, M Rocchi, et al.
Il Giornale Di Chirurgia|August 13, 1999
[Genetic factors and colorectal cancer: a new approach to clinical experimentation]G Midiri, A Tesoriere, E Giarnieri, et al.
British Journal of Haematology|January 1, 1992
Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instabilityS Filosa, V Calabrò, D Vallone, et al.
American Journal of Human Genetics|January 1, 1995
Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific)M Ganczakowski, M Town, D K Bowden, et al.
Photodermatology, Photoimmunology & Photomedicine|October 1, 1996
In vitro photoinhibition by psoralen and ultraviolet A radiation of human hematopoietic progenitorsE M Procaccini, C Selleri, G Monfrecola, et al.
British Journal of Haematology|November 1, 1987
Alpha, beta and gamma T-cell receptor genes: rearrangements correlate with haematological phenotype in T cell leukaemiasL Foroni, J Foldi, E Matutes, et al.
Molecular and Biochemical Parasitology|April 1, 1994
Cloning of the glucose 6-phosphate dehydrogenase gene from Plasmodium falciparumE O'Brien, B Kurdi-Haidar, W Wanachiwanawin, et al.
Human Genetics|November 1, 1994
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in AlgeriaK Nafa, A Reghis, N Osmani, et al.
Nucleic Acids Research|March 25, 1986
Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding regionM G Persico, G Viglietto, G Martini, et al.
Blood|August 1, 1985
Prolymphocytic leukemia of B cell type: rearranged immunoglobulin (Ig) genes with defective Ig productionJ V Melo, L Foroni, V Brito Babapulle, et al.
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