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Acta Haematologica
|
January 1, 1970
The osmotic fragility of red cells in newborns and infants
L Luzzatto, G J Esan, S E Ogiemudia
Blood
|
January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype
P Hillmen, M Bessler, D H Crawford, et al.
Leukemia & Lymphoma
|
July 28, 2016
Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic Leukaemias
A K Singh, M Laffan, S Eridani, et al.
Journal of Medical Genetics
|
July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28
R Arngrimsson, I Dokal, L Luzzatto, et al.
Lancet (London, England)
|
January 15, 1972
Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant
U Bienzle, O Ayeni, A O Lucas, et al.
Clinical and Laboratory Haematology
|
January 1, 1983
Familial erythrocytosis with over-production of erythropoietin
A Hellmann, B Rotoli, P M Cotes, et al.
British Journal of Haematology
|
August 1, 1994
Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria
M Bessler, P J Mason, P Hillmen, et al.
Blood
|
October 1, 1975
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community
U Bienzle, O Sodeinde, C E Effiong, et al.
Molecular Biology & Medicine
|
February 1, 1984
DNA rearrangements of immunoglobulin genes correlate with phenotypic markers in B-cell malignancies
L Foroni, D Catovsky, T H Rabbitts, et al.
Blood
|
October 27, 1998
New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria
K Nafa, M Bessler, H J Deeg, et al.
Page
of 26
Search research articles
Search
Showing results (101-110 of 259) with videos related to
Sort By:
Page
of 26
Acta Haematologica
|
January 1, 1970
The osmotic fragility of red cells in newborns and infants
L Luzzatto, G J Esan, S E Ogiemudia
Blood
|
January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype
P Hillmen, M Bessler, D H Crawford, et al.
Leukemia & Lymphoma
|
July 28, 2016
Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic Leukaemias
A K Singh, M Laffan, S Eridani, et al.
Journal of Medical Genetics
|
July 1, 1993
Dyskeratosis congenita: three additional families show linkage to a locus in Xq28
R Arngrimsson, I Dokal, L Luzzatto, et al.
Lancet (London, England)
|
January 15, 1972
Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant
U Bienzle, O Ayeni, A O Lucas, et al.
Clinical and Laboratory Haematology
|
January 1, 1983
Familial erythrocytosis with over-production of erythropoietin
A Hellmann, B Rotoli, P M Cotes, et al.
British Journal of Haematology
|
August 1, 1994
Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria
M Bessler, P J Mason, P Hillmen, et al.
Blood
|
October 1, 1975
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community
U Bienzle, O Sodeinde, C E Effiong, et al.
Molecular Biology & Medicine
|
February 1, 1984
DNA rearrangements of immunoglobulin genes correlate with phenotypic markers in B-cell malignancies
L Foroni, D Catovsky, T H Rabbitts, et al.
Blood
|
October 27, 1998
New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria
K Nafa, M Bessler, H J Deeg, et al.
Page
of 26