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  • Chromosomes, Human, Pair 1

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  • Disorders

    • Charcot-Marie-Tooth Disease

    • Genetic Markers

    • Alzheimer's Disease

    • Hereditary Sensory and Motor Neuropathy

    • Muscular Atrophy, Spinal

    • Alcoholism

  • Chemicals & Drugs

    • Presenilin-2

    • Apolipoproteins E

    • Presenilin-1

    • Microsatellite Repeats

    • Myelin Proteins

    • Myelin P0 Protein

    • Amyloid beta-Protein Precursor

    • Exons

  • Procedures

    • Chromosome Mapping

    • DNA Mutational Analysis

    • Genetic Testing

  • Anatomy

    • Chromosomes, Human, Pair 14

    • Chromosomes, Human, Pair 21

    • Chromosomes, Human, Pair 19

    • Chromosomes, Human, Pair 17

    • Chromosomes, Human, Pair 10

    • Chromosomes

    • Chromosomes, Human, Pair 6

    • Duffy Blood-Group System

    • Chromosomes, Human, Pair 2

    • Chromosomes, Human, Pair 3

    • Chromosomes, Human, Pair 4

    • Tooth

    • Chromosomes, Human, Pair 5

  • Physiology

    • Genetic Predisposition to Disease

    • Genotype

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    • Phenotype

    • Heritable Quantitative Trait

    • Mutation

  • Genes & Molecular Sequences

    • Single Nucleotide Polymorphism

    • Genome, Human

    • Dominant Genes

    • Alleles

    • Quantitative Trait Loci

  • Concepts & Ideas

    • Lod Score

    • Pedigree

    • Age of Onset

    • Linkage Disequilibrium

    • Family Health

  • Activities & Behaviors

    • Molecular Epidemiology

  • Occupations

    • Genetics

  • Organizations

    • National Heart, Lung, and Blood Institute (U.S.)