Search research articles
Contact Us
Filters
Showing results (151-160 of 228) with videos related to
Page
of 23
Sort By:
Genome Research
|
March 18, 2000
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human
Y Ji, N A Rebert, J M Joslin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 21, 1998
Genetic mapping of the galanin-GMAP (Galn) gene to mouse chromosome 19
L C Guida, P Charlton, D J Gilbert, et al.
American Journal of Human Genetics
|
August 1, 1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy
L M White, P K Rogan, R D Nicholls, et al.
Plos One
|
May 11, 2012
Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia
Brian J Henson, Wan Zhu, Kelsey Hardaway, et al.
European Journal of Clinical Nutrition
|
July 16, 2015
Body composition in young female eating-disorder patients with severe weight loss and controls: evidence from the four-component model and evaluation of DXA
J C K Wells, D Haroun, J E Williams, et al.
Geoscientific Model Development
|
April 27, 2018
Influence of Bulk Microphysics Schemes upon Weather Research and Forecasting (WRF) Version 3.6.1 Nor'easter Simulations
Stephen D Nicholls, Steven G Decker, Wei-Kuo Tao, et al.
Nature
|
July 29, 1993
Allele-specific replication timing of imprinted gene regions
D Kitsberg, S Selig, M Brandeis, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners
|
March 13, 2015
Comparison of local reactions to oxaliplatin infusions by peripheral versus central venous administration
Yue-Yun To, Kimberly J Sutcliffe, Helena M Hoen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 3, 2005
Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models
Feng Ding, Yelena Prints, Madhu S Dhar, et al.
Journal of Medical Genetics
|
February 27, 2004
BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications
D P Locke, R Segraves, R D Nicholls, et al.
Page
of 23
Search research articles
Search
Showing results (151-160 of 228) with videos related to
Sort By:
Page
of 23
Genome Research
|
March 18, 2000
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human
Y Ji, N A Rebert, J M Joslin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 21, 1998
Genetic mapping of the galanin-GMAP (Galn) gene to mouse chromosome 19
L C Guida, P Charlton, D J Gilbert, et al.
American Journal of Human Genetics
|
August 1, 1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy
L M White, P K Rogan, R D Nicholls, et al.
Plos One
|
May 11, 2012
Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia
Brian J Henson, Wan Zhu, Kelsey Hardaway, et al.
European Journal of Clinical Nutrition
|
July 16, 2015
Body composition in young female eating-disorder patients with severe weight loss and controls: evidence from the four-component model and evaluation of DXA
J C K Wells, D Haroun, J E Williams, et al.
Geoscientific Model Development
|
April 27, 2018
Influence of Bulk Microphysics Schemes upon Weather Research and Forecasting (WRF) Version 3.6.1 Nor'easter Simulations
Stephen D Nicholls, Steven G Decker, Wei-Kuo Tao, et al.
Nature
|
July 29, 1993
Allele-specific replication timing of imprinted gene regions
D Kitsberg, S Selig, M Brandeis, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners
|
March 13, 2015
Comparison of local reactions to oxaliplatin infusions by peripheral versus central venous administration
Yue-Yun To, Kimberly J Sutcliffe, Helena M Hoen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 3, 2005
Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models
Feng Ding, Yelena Prints, Madhu S Dhar, et al.
Journal of Medical Genetics
|
February 27, 2004
BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications
D P Locke, R Segraves, R D Nicholls, et al.
Page
of 23