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Blood
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December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
K Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics
|
May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21
M Bessler, P Hillmen, L Longo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variants
L 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 liver
O A Oluboyede, G J Esan, T I Francis, 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 Oman
S Daar, T J Vulliamy, J Kaeda, et al.
Tumori
|
August 31, 1989
Risk factors for soft tissue sarcomas in childhood: a case-control study
C Magnani, G Pastore, L Luzzatto, et al.
Human Molecular Genetics
|
May 1, 1994
The glucose-6-phosphate dehydrogenase (G6PD) deficient variant G6PD Union (454 Arg-->Cys) has a worldwide distribution possibly due to recurrent mutation
A Rovira, T J Vulliamy, A Pujades, et al.
Somatic Cell Genetics
|
July 1, 1983
Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids
M 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 activity
G Battistuzzi, G J Esan, F A Fasuan, et al.
Page
of 26
Search research articles
Search
Showing results (131-140 of 259) with videos related to
Sort By:
Page
of 26
Blood
|
December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
K Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics
|
May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21
M Bessler, P Hillmen, L Longo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variants
L 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 liver
O A Oluboyede, G J Esan, T I Francis, 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 Oman
S Daar, T J Vulliamy, J Kaeda, et al.
Tumori
|
August 31, 1989
Risk factors for soft tissue sarcomas in childhood: a case-control study
C Magnani, G Pastore, L Luzzatto, et al.
Human Molecular Genetics
|
May 1, 1994
The glucose-6-phosphate dehydrogenase (G6PD) deficient variant G6PD Union (454 Arg-->Cys) has a worldwide distribution possibly due to recurrent mutation
A Rovira, T J Vulliamy, A Pujades, et al.
Somatic Cell Genetics
|
July 1, 1983
Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids
M 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 activity
G Battistuzzi, G J Esan, F A Fasuan, et al.
Page
of 26