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    Tytuł:
    Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.
    Autorzy:
    Dewey FE; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America.
    Grove ME; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America.
    Priest JR; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Pediatric Cardiology, Stanford University, Stanford, California, United States of America.
    Waggott D; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America.
    Batra P; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America.
    Miller CL; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America.
    Wheeler M; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America.
    Zia A; Stanford Center for Genomics and Personalized Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Pan C; Stanford Center for Genomics and Personalized Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Karzcewski KJ; Stanford Center for Genomics and Personalized Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America; Biomedical Informatics Training Program, Stanford University, Stanford, California, United States of America.
    Miyake C; Division of Pediatric Cardiology, Stanford University, Stanford, California, United States of America.
    Whirl-Carrillo M; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Klein TE; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Datta S; Stanford Center for Genomics and Personalized Medicine, Stanford University, Stanford, California, United States of America.
    Altman RB; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Snyder M; Stanford Center for Genomics and Personalized Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America.
    Quertermous T; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America.
    Ashley EA; Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, United States of America; Stanford Cardiovascular Institute, Stanford University, Stanford, California, United States of America; Division of Cardiovascular Medicine, Stanford University, Stanford, California, United States of America; Department of Genetics, Stanford University, Stanford, California, United States of America.
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    Źródło:
    PLoS genetics [PLoS Genet] 2015 Oct 08; Vol. 11 (10), pp. e1005496. Date of Electronic Publication: 2015 Oct 08 (Print Publication: 2015).
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural
    MeSH Terms:
    Genetic Predisposition to Disease*
    Sequence Analysis, DNA*
    Arrhythmias, Cardiac/*genetics
    Plasma Membrane Calcium-Transporting ATPases/*genetics
    Arrhythmias, Cardiac/pathology ; Base Sequence ; Chromosome Mapping ; Genetic Variation ; Genome, Human ; Genotype ; Humans ; Phenotype
    Czasopismo naukowe
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