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European Journal of Human Genetics : EJHG|December 15, 2010
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in AustraliaManuel A R Ferreira, Allan F McRae, Sarah E Medland, et al.
Nature Genetics|July 7, 2009
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous neviMario Falchi, Veronique Bataille, Nicholas K Hayward, et al.
ACS Medicinal Chemistry Letters|November 16, 2018
Optimization of Preclinical Metabolism for Somatostatin Receptor Subtype 5-Selective AntagonistsWeiguo Liu, Zahid Hussain, Yi Zang, et al.
JACC. Cardiovascular Interventions|July 4, 2016
The Impact of Timing of Ischemic and Hemorrhagic Events on Mortality After Percutaneous Coronary Intervention: The ADAPT-DES StudySorin J Brener, Ajay J Kirtane, Thomas D Stuckey, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|November 23, 2023
GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ TwinsScott D Gordon, David L Duffy, David C Whiteman, et al.
Genome Research|October 19, 2018
Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genesTongwu Zhang, Jiyeon Choi, Michael A Kovacs, et al.
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