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  • Myotonic Dystrophy

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  • Disorders

    • Muscular Dystrophies

    • Myotonia

    • Duchenne Muscular Dystrophy

    • Myotonia Congenita

    • Trinucleotide Repeat Expansion

    • Myotonic Disorders

    • Charcot-Marie-Tooth Disease

    • Spinocerebellar Degenerations

    • Inborn Genetic Diseases

    • Chromosome Disorders

    • Alzheimer's Disease

    • Genetic Markers

    • Huntington's Disease

    • Electrocardiography

    • Congenital Structural Myopathies

  • Chemicals & Drugs

    • Trinucleotide Repeats

    • tau Proteins

    • Protein Kinases

    • Spin Labels

    • Apolipoprotein C-II

    • Spectrins

    • Protein-Serine-Threonine Kinases

    • Phosphatidic Acids

    • RNA-Binding Proteins

    • Membrane Proteins

    • DNA Restriction Enzymes

    • Apolipoproteins C

    • Glycophorin

    • Genomic Library

    • Sodium Dodecyl Sulfate

  • Procedures

    • Electron Spin Resonance Spectroscopy

    • Chromosome Mapping

    • Electrophoresis, Polyacrylamide Gel

  • Anatomy

    • Chromosomes, Human, Pair 19

    • Erythrocyte Membrane

    • Chromosomes, Human, 19-20

    • Erythrocytes

    • Cell Membrane

    • Human Chromosomes

    • Bundle of His

    • Muscles

    • Brain

  • Physiology

    • Polymorphism, Restriction Fragment Length

    • Membrane Fluidity

  • Genes & Molecular Sequences

    • Dominant Genes

  • Concepts & Ideas

    • Pedigree

    • Lod Score

  • Occupations

    • Molecular Biology

  • Phenomena

    • Phosphorylation

    • Nucleic Acid Hybridization