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The Journal of Clinical Investigation
|
August 7, 2012
Aneuploidy as a mechanism for stress-induced liver adaptation
Andrew W Duncan, Amy E Hanlon Newell, Weimin Bi, et al.
European Journal of Human Genetics : EJHG
|
November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
BMC Genomics
|
January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region
Yong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Annals of Neurology
|
March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuria
Olaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
The American Journal of Pathology
|
February 1, 2005
Receptor-mediated tobacco toxicity: regulation of gene expression through alpha3beta2 nicotinic receptor in oral epithelial cells
Juan Arredondo, Alexander I Chernyavsky, Lisa M Marubio, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation
Mark N Ziats, Mathew S Comeaux, Yaping Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2002
Involvement of the alpha3 subunit in central nicotinic binding populations
Paul Whiteaker, Cyrus G Peterson, Wei Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 9, 2005
Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vector
Gabriele Toietta, Viraj P Mane, Wilma S Norona, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2015
Corrigendum to "Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation"
Mark N Ziats, Matthew S Comeaux, Yaping Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Page
of 19
Search research articles
Search
Showing results (71-80 of 190) with videos related to
Sort By:
Page
of 19
The Journal of Clinical Investigation
|
August 7, 2012
Aneuploidy as a mechanism for stress-induced liver adaptation
Andrew W Duncan, Amy E Hanlon Newell, Weimin Bi, et al.
European Journal of Human Genetics : EJHG
|
November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
BMC Genomics
|
January 30, 2008
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region
Yong-Hui Jiang, Kekio Wauki, Qian Liu, et al.
Annals of Neurology
|
March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuria
Olaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
The American Journal of Pathology
|
February 1, 2005
Receptor-mediated tobacco toxicity: regulation of gene expression through alpha3beta2 nicotinic receptor in oral epithelial cells
Juan Arredondo, Alexander I Chernyavsky, Lisa M Marubio, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation
Mark N Ziats, Mathew S Comeaux, Yaping Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2002
Involvement of the alpha3 subunit in central nicotinic binding populations
Paul Whiteaker, Cyrus G Peterson, Wei Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 9, 2005
Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vector
Gabriele Toietta, Viraj P Mane, Wilma S Norona, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2015
Corrigendum to "Improvement of regressive autism symptoms in a child with TMLHE deficiency following carnitine supplementation"
Mark N Ziats, Matthew S Comeaux, Yaping Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Page
of 19