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International Journal of Cancer
|
May 15, 1980
Establishment in continuous culture of a T-lymphoid cell line (HD-Mar) from a patient with Hodgkin's lymphoma
H Ben-Bassat, S Mitrani-Rosenbaum, H Gamliel, et al.
Blood
|
February 1, 1980
Changes in the Con-A-induced redistribution pattern of lymphocytes: a possible aid in the differential diagnosis between malignant lymphoma and other diseases
H Ben-Bassat, S Penchas, A Polliack, et al.
British Journal of Cancer
|
February 24, 2006
Multimarker RT-PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients
A Nissan, D Jager, M Roystacher, et al.
Brain : a Journal of Neurology
|
May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features
Z Argov, M Sadeh, K Mazor, et al.
Nature Genetics
|
August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
International Journal of Cancer
|
May 15, 1980
Establishment in continuous culture of a T-lymphoid cell line (HD-Mar) from a patient with Hodgkin's lymphoma
H Ben-Bassat, S Mitrani-Rosenbaum, H Gamliel, et al.
Blood
|
February 1, 1980
Changes in the Con-A-induced redistribution pattern of lymphocytes: a possible aid in the differential diagnosis between malignant lymphoma and other diseases
H Ben-Bassat, S Penchas, A Polliack, et al.
British Journal of Cancer
|
February 24, 2006
Multimarker RT-PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients
A Nissan, D Jager, M Roystacher, et al.
Brain : a Journal of Neurology
|
May 29, 2000
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features
Z Argov, M Sadeh, K Mazor, et al.
Nature Genetics
|
August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Page
of 5