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Human Mutation
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January 15, 2004
Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsy
Leonarda Ianzano, Edwin J Young, Xiao C Zhao, et al.
Genome Medicine
|
April 4, 2009
The cycle of genome-directed medicine
Janet A Buchanan, Andrew R Carson, David Chitayat, et al.
Genome Research
|
March 1, 1996
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31
P Höglund, S Haila, S W Scherer, et al.
Chemosphere
|
May 4, 2010
Effect of long term organic amendments on adsorption-desorption of thiram onto a luvisol soil derived from loess
O M S Filipe, M M Vidal, H W Scherer, et al.
The Journal of Pediatrics
|
January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
Grace Yoon, Zeenat Malam, Tara Paton, et al.
BMC Medical Genetics
|
March 29, 2011
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
Mohammad M Ghahramani Seno, Benjamin Y M Kwan, Ka Ki M Lee-Ng, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
August 10, 2011
Evolution of quantum criticality in CeNi(9-x)Cu(x)Ge(4)
L Peyker, C Gold, E-W Scheidt, et al.
The Journal of Biological Chemistry
|
August 15, 1993
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene
P A Marsden, H H Heng, S W Scherer, et al.
Gene
|
September 5, 1998
Genomic structure of the human congenital chloride diarrhea (CLD) gene
S Haila, P Höglund, S W Scherer, et al.
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
September 26, 1997
Delineation of genomic regions in chromosome band 7q22 commonly deleted in myeloid leukemias
K Fischer, J Brown, S W Scherer, et al.
Page
of 92
Search research articles
Search
Showing results (481-490 of 915) with videos related to
Sort By:
Page
of 92
Human Mutation
|
January 15, 2004
Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsy
Leonarda Ianzano, Edwin J Young, Xiao C Zhao, et al.
Genome Medicine
|
April 4, 2009
The cycle of genome-directed medicine
Janet A Buchanan, Andrew R Carson, David Chitayat, et al.
Genome Research
|
March 1, 1996
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31
P Höglund, S Haila, S W Scherer, et al.
Chemosphere
|
May 4, 2010
Effect of long term organic amendments on adsorption-desorption of thiram onto a luvisol soil derived from loess
O M S Filipe, M M Vidal, H W Scherer, et al.
The Journal of Pediatrics
|
January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
Grace Yoon, Zeenat Malam, Tara Paton, et al.
BMC Medical Genetics
|
March 29, 2011
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
Mohammad M Ghahramani Seno, Benjamin Y M Kwan, Ka Ki M Lee-Ng, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
August 10, 2011
Evolution of quantum criticality in CeNi(9-x)Cu(x)Ge(4)
L Peyker, C Gold, E-W Scheidt, et al.
The Journal of Biological Chemistry
|
August 15, 1993
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene
P A Marsden, H H Heng, S W Scherer, et al.
Gene
|
September 5, 1998
Genomic structure of the human congenital chloride diarrhea (CLD) gene
S Haila, P Höglund, S W Scherer, et al.
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
September 26, 1997
Delineation of genomic regions in chromosome band 7q22 commonly deleted in myeloid leukemias
K Fischer, J Brown, S W Scherer, et al.
Page
of 92