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G3 (Bethesda, Md.)
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March 3, 2012
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics
Mahdi Ghani, Dalila Pinto, Joseph H Lee, et al.
Human Mutation
|
April 13, 2016
Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts
Rita Y Y Yong, Su'Aidah B Mustaffa, Pavandip S Wasan, et al.
American Journal of Medical Genetics
|
July 13, 2002
Genetic analysis of patients with the Saethre-Chotzen phenotype
Kathy Chun, Ahmad S Teebi, Jack H Jung, et al.
Acta Crystallographica. Section B, Structural Science
|
August 1, 2002
Reproducability and transferability of topological properties; experimental charge density of the hexapeptide cyclo-(D,L-Pro)2-(L-Ala)4 monohydrate
B Dittrich, T Koritsánszky, M Grosche, et al.
Global Challenges (Hoboken, NJ)
|
October 1, 2019
Study of Toxic Elements in River Water and Wetland Using Water Hyacinth (<i>Eichhornia crassipes)</i> as Pollution Monitor
Alok Srivastava, Vikas Chahar, Vishal Sharma, et al.
Genome Research
|
October 1, 1995
A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines
K Torigoe, S Sato, H Kusaba, et al.
Genomics
|
May 8, 1998
Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1
K Torigoe, T Harada, H Kusaba, et al.
American Journal of Medical Genetics. Part A
|
July 5, 2016
Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome
Cheryl Cytrynbaum, Karen Chong, Vickie Hannig, et al.
Controlled Clinical Trials
|
May 22, 2003
Surgical quality assurance in the Ischemic Optic Neuropathy Decompression Trial (IONDT)
Steven E Feldon, Roberta W Scherer, Frank J Hooper, et al.
Nature Genetics
|
October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
L R Osborne, M Li, B Pober, et al.
Page
of 92
Search research articles
Search
Showing results (501-510 of 915) with videos related to
Sort By:
Page
of 92
G3 (Bethesda, Md.)
|
March 3, 2012
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics
Mahdi Ghani, Dalila Pinto, Joseph H Lee, et al.
Human Mutation
|
April 13, 2016
Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts
Rita Y Y Yong, Su'Aidah B Mustaffa, Pavandip S Wasan, et al.
American Journal of Medical Genetics
|
July 13, 2002
Genetic analysis of patients with the Saethre-Chotzen phenotype
Kathy Chun, Ahmad S Teebi, Jack H Jung, et al.
Acta Crystallographica. Section B, Structural Science
|
August 1, 2002
Reproducability and transferability of topological properties; experimental charge density of the hexapeptide cyclo-(D,L-Pro)2-(L-Ala)4 monohydrate
B Dittrich, T Koritsánszky, M Grosche, et al.
Global Challenges (Hoboken, NJ)
|
October 1, 2019
Study of Toxic Elements in River Water and Wetland Using Water Hyacinth (<i>Eichhornia crassipes)</i> as Pollution Monitor
Alok Srivastava, Vikas Chahar, Vishal Sharma, et al.
Genome Research
|
October 1, 1995
A YAC-based contig of 1.5 Mb spanning the human multidrug resistance gene region and delineating the amplification unit in three human multidrug-resistant cell lines
K Torigoe, S Sato, H Kusaba, et al.
Genomics
|
May 8, 1998
Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1
K Torigoe, T Harada, H Kusaba, et al.
American Journal of Medical Genetics. Part A
|
July 5, 2016
Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome
Cheryl Cytrynbaum, Karen Chong, Vickie Hannig, et al.
Controlled Clinical Trials
|
May 22, 2003
Surgical quality assurance in the Ischemic Optic Neuropathy Decompression Trial (IONDT)
Steven E Feldon, Roberta W Scherer, Frank J Hooper, et al.
Nature Genetics
|
October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
L R Osborne, M Li, B Pober, et al.
Page
of 92