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Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24
M A Crackower, D S Sinasac, J R Lee, et al.
Blood
|
May 1, 1996
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia
E J Johnson, S W Scherer, L Osborne, et al.
Genes, Chromosomes & Cancer
|
August 19, 1999
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization
S Tosi, G Giudici, A Rambaldi, et al.
Neurology
|
August 12, 2004
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locus
E M Chan, S Omer, M Ahmed, et al.
Oncogene
|
May 15, 1997
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas
W R Zeng, S W Scherer, M Koutsilieris, et al.
American Journal of Human Genetics
|
August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome
L R Osborne, S Soder, X M Shi, et al.
Atherosclerosis
|
August 12, 1998
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites
A P Boright, P W Connelly, J H Brunt, et al.
Cancer Genetics and Cytogenetics
|
April 13, 1999
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype
M G de Silva, P Kantharidis, S W Scherer, et al.
The Journal of Biological Chemistry
|
September 15, 1995
Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families
E A Barron-Casella, M A Torres, S W Scherer, et al.
Neurology
|
August 10, 2000
Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy
B A Minassian, L Ianzano, M Meloche, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 164) with videos related to
Sort By:
Page
of 17
Cytogenetics and Cell Genetics
|
March 7, 2000
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24
M A Crackower, D S Sinasac, J R Lee, et al.
Blood
|
May 1, 1996
Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia
E J Johnson, S W Scherer, L Osborne, et al.
Genes, Chromosomes & Cancer
|
August 19, 1999
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization
S Tosi, G Giudici, A Rambaldi, et al.
Neurology
|
August 12, 2004
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locus
E M Chan, S Omer, M Ahmed, et al.
Oncogene
|
May 15, 1997
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas
W R Zeng, S W Scherer, M Koutsilieris, et al.
American Journal of Human Genetics
|
August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome
L R Osborne, S Soder, X M Shi, et al.
Atherosclerosis
|
August 12, 1998
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites
A P Boright, P W Connelly, J H Brunt, et al.
Cancer Genetics and Cytogenetics
|
April 13, 1999
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype
M G de Silva, P Kantharidis, S W Scherer, et al.
The Journal of Biological Chemistry
|
September 15, 1995
Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families
E A Barron-Casella, M A Torres, S W Scherer, et al.
Neurology
|
August 10, 2000
Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy
B A Minassian, L Ianzano, M Meloche, et al.
Page
of 17