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Refinado por: Nome da Publicação: Human Genetics remover
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1
Advances in hereditary red cell enzyme anomalies
Advances in hereditary red cell enzyme anomalies
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Advances in hereditary red cell enzyme anomalies

Kahn, A ; Kaplan, J C ; Dreyfus, J C

Human genetics, 1979-01, Vol.50 (1), p.1-27 [Periódico revisado por pares]

Germany

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2
Gene dosage effect in human triploid fibroblasts
Gene dosage effect in human triploid fibroblasts
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Gene dosage effect in human triploid fibroblasts

Junien, C ; Rubinson, H ; Dreyfus, J C ; Meinenhofer, M C ; Ravise, N ; Boué, J ; Boué, A

Human genetics, 1976-01, Vol.33 (1), p.61-66 [Periódico revisado por pares]

Germany

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3
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance
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PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance

Junien, C ; Rubinson-Skala, H ; Dreyfus, J C ; Ravise, N ; Boué, J ; Boué, A ; Kaplan, J C

Human genetics, 1980, Vol.54 (2), p.191-196 [Periódico revisado por pares]

Germany

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4
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants
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Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants

Benabadji, M ; Merad, F ; Benmoussa, M ; Trabuchet, G ; Junien, C ; Dreyfus, J C ; Kaplan, J C

Human genetics, 1978-01, Vol.40 (2), p.177-184 [Periódico revisado por pares]

Germany

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5
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting technique
Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting technique
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Evidence for the presence of beta-subunit of hexosaminidase in a case of Sandhoff disease using a blotting technique

Gautron, S ; Poenaru, L ; Boue, J ; Puissant, H ; Lisman, J J ; Dreyfus, J C

Human genetics, 1983, Vol.63 (3), p.258-261 [Periódico revisado por pares]

Germany

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6
Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain
Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain
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Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain

Vives-Corrons, J L ; Rubinson-Skala, H ; Mateo, M ; Estella, J ; Feliu, E ; Dreyfus, J C

Human genetics, 1978-01, Vol.42 (2), p.171-180 [Periódico revisado por pares]

Germany

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7
Phosphofructokinase (PFK) isozymes in man. I. Studies of adult human tissues
Phosphofructokinase (PFK) isozymes in man. I. Studies of adult human tissues
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Phosphofructokinase (PFK) isozymes in man. I. Studies of adult human tissues

Kahn, A ; Meienhofer, M C ; Cottreau, D ; Lagrange, J L ; Dreyfus, J C

Human genetics, 1979-04, Vol.48 (1), p.93-108 [Periódico revisado por pares]

Germany

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