L Luzzatto|S M Gartler - JoVE Visualize

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Leukemia & Lymphoma|July 28, 2016

Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic LeukaemiasA 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 Xq28R Arngrimsson, I Dokal, L Luzzatto, et al.

Clinical and Laboratory Haematology|January 1, 1983

Familial erythrocytosis with over-production of erythropoietinA 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 haemoglobinuriaM 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 communityU 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 malignanciesL 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 hemoglobinuriaK Nafa, M Bessler, H J Deeg, et al.

Molecular Biology & Medicine|April 1, 1984

Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenaseD Toniolo, M G Persico, G Battistuzzi, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 29, 1999

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individualsD J Araten, K Nafa, K Pakdeesuwan, et al.

The Biochemical Journal|October 1, 1990

Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNAV Poggi, M Town, N S Foulkes, et al.

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Showing results (91-100 of 237) with videos related to

Sort By:

Pageof 24

Leukemia & Lymphoma|July 28, 2016

Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic LeukaemiasA 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 Xq28R Arngrimsson, I Dokal, L Luzzatto, et al.

Clinical and Laboratory Haematology|January 1, 1983

Familial erythrocytosis with over-production of erythropoietinA 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 haemoglobinuriaM 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 communityU 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 malignanciesL 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 hemoglobinuriaK Nafa, M Bessler, H J Deeg, et al.

Molecular Biology & Medicine|April 1, 1984

Partial purification and characterization of the messenger RNA for human glucose-6-phosphate dehydrogenaseD Toniolo, M G Persico, G Battistuzzi, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 29, 1999

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individualsD J Araten, K Nafa, K Pakdeesuwan, et al.

The Biochemical Journal|October 1, 1990

Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNAV Poggi, M Town, N S Foulkes, et al.

Pageof 24