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International Journal of Cancer
|
November 15, 1990
Evidence for the role of 34-kDa galactoside-binding lectin in transformation and metastasis
A Raz, D G Zhu, V Hogan, et al.
Human Genetics
|
December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity
T Raz, T Barrett, R Szargel, et al.
American Journal of Medical Genetics
|
January 8, 1999
Atrichia with papular lesions maps to 8p in the region containing the human hairless gene
E Sprecher, R Bergman, R Szargel, et al.
American Journal of Human Genetics
|
December 18, 1997
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping
E J Neufeld, H Mandel, T Raz, et al.
Nature Genetics
|
July 3, 1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
V Labay, T Raz, D Baron, et al.
Oncogene
|
August 9, 2007
Quantitative monitoring by polymerase colony assay of known mutations resistant to ABL kinase inhibitors
V Nardi, T Raz, X Cao, et al.
Human Mutation
|
June 30, 2000
The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families
T Raz, V Labay, D Baron, et al.
Page
of 4
Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
International Journal of Cancer
|
November 15, 1990
Evidence for the role of 34-kDa galactoside-binding lectin in transformation and metastasis
A Raz, D G Zhu, V Hogan, et al.
Human Genetics
|
December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity
T Raz, T Barrett, R Szargel, et al.
American Journal of Medical Genetics
|
January 8, 1999
Atrichia with papular lesions maps to 8p in the region containing the human hairless gene
E Sprecher, R Bergman, R Szargel, et al.
American Journal of Human Genetics
|
December 18, 1997
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping
E J Neufeld, H Mandel, T Raz, et al.
Nature Genetics
|
July 3, 1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness
V Labay, T Raz, D Baron, et al.
Oncogene
|
August 9, 2007
Quantitative monitoring by polymerase colony assay of known mutations resistant to ABL kinase inhibitors
V Nardi, T Raz, X Cao, et al.
Human Mutation
|
June 30, 2000
The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families
T Raz, V Labay, D Baron, et al.
Page
of 4