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Human Heredity|January 1, 1976
Distribution of G6PD types in the population of southwest France: common variants and new variantsM Gherardi, R Bierme, J Corberand, et al.Human Genetics|January 1, 1981
Gd(-) Muret and gd(-) Colomiers, two new variants of glucose-6-phosphate dehydrogenase associated with favismH Vergnes, A Ribet, G Bommelaer, et al.American Journal of Clinical Pathology|August 1, 1978
Chronic granulomatous disease with leukocytic glucose-6-phosphate dehydrogenase deficiency in a 28-month-old girlJ Corberand, B De Larrard, H Vergnes, et al.British Journal of Haematology|February 1, 1992
Phosphotyrosine phosphatase activity and haematologic changes in Down's syndrome patientsH Vergnes, A Brisson-Lougarre, P Limouzy, et al.Human Heredity|January 1, 1979
Genetic variants of human glucose-6-phosphate dehydrogenase in a Saharian and Pygmy familyH Vergnes, M Gherardi, P Lefevre-Witier, et al.Annals of Human Biology|November 1, 1979
Methaemoglobin and erythrocyte reducing systems in high-altitude nativesJ Arnaud, J C Quilici, N Gutierrez, et al.Enzyme|January 1, 1992
Alkaline phosphatase and phosphotyrosine phosphatase activities of cultured amniotic cells with trisomy 18H Vergnes, J Grozdea, A Brisson-Lougarre, et al.Human Heredity|January 1, 1980
Study of red blood cell and serum enzymes in five Pyrenean communities and in a Basque population sampleH Vergnes, J Constans, J C Quilici, et al.Human Heredity|January 1, 1980
Erythrocyte glyoxalase I and esterase D polymorphisms in four French populationsH Vergnes, S Meyer, D Weil, et al.Acta Haematologica|January 1, 1994
Changes in immunological properties of neutrophil alkaline phosphatase in trisomy 21 pregnanciesJ Grozdea, H Vergnes, A Brisson-Lougarre, et al.Pageof 5