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  • Chromosomes, Human, Pair 17

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  • Disorders

    • Frontotemporal Dementia

    • Dementia

    • Parkinsonian Disorders

    • Charcot-Marie-Tooth Disease

    • Genetic Markers

    • Parkinson's Disease

    • Tauopathies

    • Brachial Plexus Neuritis

    • Supranuclear Palsy, Progressive

    • Alzheimer's Disease

    • Hereditary Sensory and Motor Neuropathy

    • Neurofibrillary Tangles

    • Neurofibromatosis 1

    • Neurodegenerative Diseases

    • Neurofibromatoses

    • Pick Disease of the Brain

    • Nerve Degeneration

    • Paralysis

  • Chemicals & Drugs

    • tau Proteins

    • Microtubule Associated Proteins

    • Exons

    • Myelin Proteins

    • Alternative Splicing

    • Protein Isoforms

    • Myelin P0 Protein

    • Nerve Tissue Proteins

    • Introns

    • Synucleins

  • Procedures

    • Chromosome Mapping

    • DNA Mutational Analysis

  • Anatomy

    • Frontal Lobe

    • Temporal Lobe

    • Microtubules

    • Chromosomes

    • Chromosomes, Human, Pair 1

    • Chromosomes, Human, Pair 22

  • Physiology

    • Mutation

    • Missense Mutation

    • Haplotypes

    • Point Mutation

    • Genotype

    • Genetic Predisposition to Disease

    • Polymorphism, Restriction Fragment Length

  • Genes & Molecular Sequences

    • Dominant Genes

    • Multigene Family

  • Concepts & Ideas

    • Pedigree

    • Lod Score

    • Age of Onset

    • Family Health

    • Gene Frequency