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  • Haplotypes

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  • Disorders

    • Genetic Markers

    • Alzheimer's Disease

    • Charcot-Marie-Tooth Disease

    • Parkinson's Disease

    • Supranuclear Palsy, Progressive

    • Frontotemporal Dementia

    • Huntington's Disease

    • Dementia

    • Parkinsonian Disorders

    • Amyotrophic Lateral Sclerosis

  • Chemicals & Drugs

    • tau Proteins

    • Apolipoproteins E

    • Microsatellite Repeats

    • Apolipoprotein E4

    • Nerve Tissue Proteins

    • Repetitive Sequences, Nucleic Acid

    • Synucleins

    • alpha-Synuclein

    • Exons

  • Procedures

    • Chromosome Mapping

    • DNA Mutational Analysis

    • Case Control Studies

    • Genetic Testing

    • Contig Mapping

  • Anatomy

    • Chromosomes

    • Chromosomes, Human, Pair 17

    • Chromosomes, Human, Pair 8

    • Chromosomes, Human, Pair 2

    • Chromosomes, Human, Pair 4

    • Chromosomes, Human, Pair 9

    • Human Chromosomes

  • Physiology

    • Genotype

    • Genetic Predisposition to Disease

    • Polymorphism, Restriction Fragment Length

    • Genetic Heterogeneity

    • Mutation

    • Phenotype

    • Recombination, Genetic

  • Genes & Molecular Sequences

    • Alleles

    • Single Nucleotide Polymorphism

    • Dominant Genes

    • Recessive Genes

  • Concepts & Ideas

    • Pedigree

    • Linkage Disequilibrium

    • Lod Score

    • Age of Onset

    • Gene Frequency

    • Family Health

  • Phenomena

    • Founder Effect

  • Devices

    • Yeast Artificial Chromosomes