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American Journal of Human Genetics
|
November 1, 1981
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect
C R Bartram, H W Rüdiger, U Schmidt-Preuss, et al.
Bioelectromagnetics
|
December 21, 2000
Single, brief exposure to a 50 Hz magnetic field does not affect the performance of an object recognition task in adult mice
Z J Sienkiewicz, R Bartram, R G Haylock, et al.
Human Genetics
|
January 1, 1981
Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factor
U Schmidt-Preuss, P Maack, C R Bartram, et al.
Leukemia
|
August 1, 1993
SIL-TAL1 deletion in T-cell acute lymphoblastic leukemia
J W Janssen, W D Ludwig, W Sterry, et al.
Oncogene
|
May 1, 1987
Novel transforming sequences in human acute myelocytic leukemia cell lines
J W Janssen, A C Steenvoorden, M Losekoot, et al.
Human Genetics
|
January 28, 1999
Mutations in the gene for the common gamma chain (gammac) in X-linked severe combined immunodeficiency
S D Fugmann, S Müller, W Friedrich, et al.
Leukemia
|
March 17, 2000
Tandem duplication of the FLT3 gene in acute lymphoblastic leukemia: a marker for the monitoring of minimal residual disease
M Nakao, J W Janssen, D Erz, et al.
British Journal of Haematology
|
December 1, 1988
Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)
A E Kulozik, J Lyons, E Kohne, et al.
The New England Journal of Medicine
|
May 23, 1985
c-abl Oncogene and chromosome 22 "bcr" juxtaposition in chronic myelogenous leukemia
J R Teyssier, C R Bartram, J Deville, et al.
Nature Biotechnology
|
September 12, 2007
Ethical framework for previously collected biobank samples
Gert Helgesson, Joakim Dillner, Joyce Carlson, et al.
Page
of 40
Search research articles
Search
Showing results (91-100 of 393) with videos related to
Sort By:
Page
of 40
American Journal of Human Genetics
|
November 1, 1981
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect
C R Bartram, H W Rüdiger, U Schmidt-Preuss, et al.
Bioelectromagnetics
|
December 21, 2000
Single, brief exposure to a 50 Hz magnetic field does not affect the performance of an object recognition task in adult mice
Z J Sienkiewicz, R Bartram, R G Haylock, et al.
Human Genetics
|
January 1, 1981
Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factor
U Schmidt-Preuss, P Maack, C R Bartram, et al.
Leukemia
|
August 1, 1993
SIL-TAL1 deletion in T-cell acute lymphoblastic leukemia
J W Janssen, W D Ludwig, W Sterry, et al.
Oncogene
|
May 1, 1987
Novel transforming sequences in human acute myelocytic leukemia cell lines
J W Janssen, A C Steenvoorden, M Losekoot, et al.
Human Genetics
|
January 28, 1999
Mutations in the gene for the common gamma chain (gammac) in X-linked severe combined immunodeficiency
S D Fugmann, S Müller, W Friedrich, et al.
Leukemia
|
March 17, 2000
Tandem duplication of the FLT3 gene in acute lymphoblastic leukemia: a marker for the monitoring of minimal residual disease
M Nakao, J W Janssen, D Erz, et al.
British Journal of Haematology
|
December 1, 1988
Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)
A E Kulozik, J Lyons, E Kohne, et al.
The New England Journal of Medicine
|
May 23, 1985
c-abl Oncogene and chromosome 22 "bcr" juxtaposition in chronic myelogenous leukemia
J R Teyssier, C R Bartram, J Deville, et al.
Nature Biotechnology
|
September 12, 2007
Ethical framework for previously collected biobank samples
Gert Helgesson, Joakim Dillner, Joyce Carlson, et al.
Page
of 40