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American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|
March 4, 2025
The impact of change in regulations on buprenorphine prescribing for opioid use disorder
Evon Ibrahim, Kaitlyn DeHoff, Eric Lambart, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2010
Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections
Siddharth Prakash, Scott A LeMaire, Molly Bray, et al.
Genetic Epidemiology
|
March 29, 2002
LPL polymorphism predicts stroke risk in men
Alanna C Morrison, Christie M Ballantyne, Molly Bray, et al.
Physiological Genomics
|
November 20, 2008
Gene expression in the human mammary epithelium during lactation: the milk fat globule transcriptome
Patricia D Maningat, Partha Sen, Monique Rijnkels, et al.
American Journal of Human Genetics
|
April 2, 2002
A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
Xiaodong Wu, Richard S Cooper, Ingrid Borecki, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2008
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
Brett T Chiquet, Syed S Hashmi, Robin Henry, et al.
Behavioural Brain Research
|
April 21, 2011
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition
Steffie N Tomson, Nili Avidan, Kwanghyuk Lee, et al.
Epidemiology (Cambridge, Mass.)
|
July 16, 2003
Risk of atherosclerosis: interaction of smoking and glutathione S-transferase genes
Andrew F Olshan, Rongling Li, James S Pankow, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2012
Altered DNA methylation profile in idiopathic pulmonary fibrosis
Yan Y Sanders, Namasivayam Ambalavanan, Brian Halloran, et al.
American Journal of Human Genetics
|
March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa
Hui Wang, Anneke I den Hollander, Yalda Moayedi, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|
March 4, 2025
The impact of change in regulations on buprenorphine prescribing for opioid use disorder
Evon Ibrahim, Kaitlyn DeHoff, Eric Lambart, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2010
Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections
Siddharth Prakash, Scott A LeMaire, Molly Bray, et al.
Genetic Epidemiology
|
March 29, 2002
LPL polymorphism predicts stroke risk in men
Alanna C Morrison, Christie M Ballantyne, Molly Bray, et al.
Physiological Genomics
|
November 20, 2008
Gene expression in the human mammary epithelium during lactation: the milk fat globule transcriptome
Patricia D Maningat, Partha Sen, Monique Rijnkels, et al.
American Journal of Human Genetics
|
April 2, 2002
A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
Xiaodong Wu, Richard S Cooper, Ingrid Borecki, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2008
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
Brett T Chiquet, Syed S Hashmi, Robin Henry, et al.
Behavioural Brain Research
|
April 21, 2011
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition
Steffie N Tomson, Nili Avidan, Kwanghyuk Lee, et al.
Epidemiology (Cambridge, Mass.)
|
July 16, 2003
Risk of atherosclerosis: interaction of smoking and glutathione S-transferase genes
Andrew F Olshan, Rongling Li, James S Pankow, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2012
Altered DNA methylation profile in idiopathic pulmonary fibrosis
Yan Y Sanders, Namasivayam Ambalavanan, Brian Halloran, et al.
American Journal of Human Genetics
|
March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa
Hui Wang, Anneke I den Hollander, Yalda Moayedi, et al.
Page
of 2