Showing results (2181-2190 of 2,287) with videos related to

Sort By:
Pageof 229
American Journal of Medical Genetics. Part A|October 21, 2016
Creation of an international registry to support discovery in schwannomatosisK L Ostrow, A L Bergner, J Blakeley, et al.
British Journal of Cancer|October 4, 2006
Cost-effectiveness of screening with contrast enhanced magnetic resonance imaging vs X-ray mammography of women at a high familial risk of breast cancerI Griebsch, J Brown, C Boggis, et al.
Science Advances|July 24, 2024
Optical and electronic functionality arising from controlled defect formation in nanoscale complex oxide lateral epitaxyRui Liu, Tesia D Janicki, Samuel D Marks, et al.
Cancers|December 17, 2024
Characterization of Somatostatin Receptor 2 Gene Expression and Immune Landscape in Sinonasal MalignanciesElisabetta Xue, Dara Bracken-Clarke, Harris Krause, et al.
Science (New York, N.Y.)|October 1, 2011
Radioactive elements on Mercury's surface from MESSENGER: implications for the planet's formation and evolutionPatrick N Peplowski, Larry G Evans, Steven A Hauck, et al.
Thrombosis and Haemostasis|May 6, 2020
A Novel, Enriched Population Pharmacokinetic Model for Recombinant Factor VIII-Fc Fusion Protein Concentrate in Hemophilia A PatientsLaura H Bukkems, Jessica M Heijdra, Mary Mathias, et al.
Veterinary Pathology|July 11, 2013
Meeting report: Emerging respiratory viral infections and nonhuman primate case reportsV G Sasseville, J L Mankowski, A Baldessari, et al.
Nano Letters|May 6, 2024
Ultrafast Optically Induced Perturbation of Oxygen Octahedral Rotations in Multiferroic BiFeO3 Thin FilmsNi Li, Hyeon Jun Lee, Deepankar Sri Gyan, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
American Journal of Human Genetics|December 13, 2006
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlationM Upadhyaya, S M Huson, M Davies, et al.
Pageof 229