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Human Molecular Genetics|January 4, 2001
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasiaP Q Thomas, M T Dattani, J M Brickman, et al.
Elife|March 29, 2023
Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traitsJoshua K Park, Shantanu Bafna, Iain S Forrest, et al.
Nature Genetics|September 18, 2007
Population genomics of human gene expressionBarbara E Stranger, Alexandra C Nica, Matthew S Forrest, et al.
Chemico-Biological Interactions|June 7, 2005
Use of 'Omic' technologies to study humans exposed to benzeneMartyn T Smith, Roel Vermeulen, Guilan Li, et al.
Frontiers in Veterinary Science|April 11, 2022
Rapid Detection of Actinobacillus pleuropneumoniae From Clinical Samples Using Recombinase Polymerase AmplificationOliver W Stringer, Yanwen Li, Janine T Bossé, et al.
Med (New York, N.Y.)|May 28, 2026
Capturing multi-disease states on a spectrum with machine learning and routine clinical dataIain S Forrest, Ben O Petrazzini, Robert Chen, et al.
Prostate Cancer and Prostatic Diseases|February 16, 2005
Association between hormonal genetic polymorphisms and early-onset prostate cancerM S Forrest, S M Edwards, R Houlston, et al.
Journal of the American Heart Association|October 29, 2021
Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart FailureIshan Paranjpe, Noah L Tsao, Jessica K De Freitas, et al.
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