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Genome Medicine|April 14, 2025
Systematic identification of disease-causing promoter and untranslated region variants in 8040 undiagnosed individuals with rare diseaseAlexandra C Martin-Geary, Alexander J M Blakes, Ruebena Dawes, et al.
The American Journal of Surgical Pathology|January 12, 2018
Parafibromin-deficient (HPT-JT Type, CDC73 Mutated) Parathyroid Tumors Demonstrate Distinctive Morphologic FeaturesAnthony J Gill, Grace Lim, Veronica K Y Cheung, et al.
European Journal of Cancer (Oxford, England : 1990)|September 7, 2000
Causes of inconsistency in diagnosing and classifying intraductal proliferations of the breast. European Commission Working Group on Breast Screening PathologyC W Elston, J P Sloane, I Amendoeira, et al.
Infectious Diseases and Therapy|July 11, 2023
Patient Biochemistry and Treatment Need in Chronic Hepatitis B Virus Infection Across Three Continents: Retrospective Cross-Sectional Cohort StudiesIain A Gillespie, Eleanor Barnes, Ian C K Wong, et al.
Cancer Research|February 12, 2005
Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHITGarry P Larson, Yan Ding, Li S-C Cheng, et al.
Cancer Research|June 17, 2010
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22Courtney Gray-McGuire, Kishore Guda, Indra Adrianto, et al.
Human Mutation|July 18, 2025
Whole Genome Sequencing of "Mutation-Negative" Individuals With Cornelia de Lange SyndromeMorad Ansari, Mihail Halachev, David Parry, et al.
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