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American Journal of Epidemiology
|
May 13, 2017
Acute Illness Among Surfers After Exposure to Seawater in Dry- and Wet-Weather Conditions
Benjamin F Arnold, Kenneth C Schiff, Ayse Ercumen, et al.
BMC Physiology
|
October 12, 2010
Identification of differences in human and great ape phytanic acid metabolism that could influence gene expression profiles and physiological functions
Paul A Watkins, Ann B Moser, Cicely B Toomer, et al.
Molecular Genetics and Metabolism
|
February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder
Shandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
American Journal of Human Genetics
|
May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders
Deyanira Corzo, William Gibson, Kisha Johnson, et al.
American Journal of Human Genetics
|
December 9, 2017
Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder
Kim D Falkenberg, Nancy E Braverman, Ann B Moser, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
American Journal of Epidemiology
|
May 13, 2017
Acute Illness Among Surfers After Exposure to Seawater in Dry- and Wet-Weather Conditions
Benjamin F Arnold, Kenneth C Schiff, Ayse Ercumen, et al.
BMC Physiology
|
October 12, 2010
Identification of differences in human and great ape phytanic acid metabolism that could influence gene expression profiles and physiological functions
Paul A Watkins, Ann B Moser, Cicely B Toomer, et al.
Molecular Genetics and Metabolism
|
February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder
Shandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
American Journal of Human Genetics
|
May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders
Deyanira Corzo, William Gibson, Kisha Johnson, et al.
American Journal of Human Genetics
|
December 9, 2017
Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder
Kim D Falkenberg, Nancy E Braverman, Ann B Moser, et al.
Page
of 3