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British Journal of Cancer|April 9, 2026
Genetic landscape of stage II melanoma identifies CBL as a new driver gene and prognostic biomarkerElena Sophia Lindner, Jakob Admard, German Demidov, et al.Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|March 27, 2020
PET/MRI and genetic intrapatient heterogeneity in head and neck cancersKerstin Clasen, Sara Leibfarth, Franz J Hilke, et al.Human Mutation|April 14, 2016
High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder AllelesSven Günther, Ewelina Elert-Dobkowska, Anne S Soehn, et al.The Journal of Allergy and Clinical Immunology|February 18, 2010
Infant-onset eczema in relation to mental health problems at age 10 years: results from a prospective birth cohort study (German Infant Nutrition Intervention plus)Jochen Schmitt, Christian Apfelbacher, Chih-Mei Chen, et al.European Journal of Human Genetics : EJHG|December 12, 2019
Novel clinical and genetic insight into CXorf56-associated intellectual disabilityMaria Eugenia Rocha, Tainá Regina Damaceno Silveira, Erina Sasaki, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|August 20, 2010
Five-grass pollen 300IR SLIT tablets: efficacy and safety in children and adolescentsSusanne Halken, Lone Agertoft, Jürgen Seidenberg, et al.Journal of Public Health Dentistry|September 14, 2012
Proportion and extent of manifestation of molar-incisor-hypomineralizations according to different phenotypesJan Kühnisch, Daniela Heitmüller, Elisabeth Thiering, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 30, 2010
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindredsPeter Bauer, Giovanni Stevanin, Christian Beetz, et al.Frontiers in Oncology|March 18, 2021
Case Report: Combined CDK4/6 and MEK Inhibition in Refractory CDKN2A and NRAS Mutant MelanomaAndrea Forschner, Tobias Sinnberg, Gabi Mroz, et al.Cytotherapy|July 29, 2019
Low mutational load in pediatric medulloblastoma still translates into neoantigens as targets for specific T-cell immunotherapyFranziska Blaeschke, Milan Cedric Paul, Martin Ulrich Schuhmann, et al.Pageof 67