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  • Chromosomes, Human, Pair 19

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  • Disorders

    • Alzheimer's Disease

    • Myotonic Dystrophy

    • Genetic Markers

    • DNA Repeat Expansion

    • Muscular Dystrophies

    • CADASIL

    • Chromosome Disorders

  • Chemicals & Drugs

    • Apolipoproteins E

    • Apolipoprotein E4

    • Amyloid beta-Protein Precursor

    • DNA Probes

    • Type II Site Specific Deoxyribonucleases

    • Microsatellite Repeats

    • Amyloid beta-Peptides

    • Xeroderma Pigmentosum Group D Protein

    • Base Sequence

    • Presenilin-2

  • Procedures

    • Chromosome Mapping

    • Genome Wide Association Studies

    • Fluorescence In Situ Hybridization

  • Anatomy

    • Chromosomes, Human, Pair 21

    • Chromosomes, Human, Pair 14

    • Chromosomes, Human, Pair 1

    • Chromosomes, Human, Pair 9

    • Human Chromosomes

    • Chromosomes

    • Chromosomes, Human, Pair 7

    • Chromosomes, Human, Pair 12

    • Hybrid Cells

    • Chromosomes, Human, 19-20

    • Chromosomes, Human, Pair 18

    • Chromosomes, Human, Pair 20

    • Chromosomes, Human, Pair 15

    • Chromosomes, Human, Pair 16

  • Physiology

    • Genetic Predisposition to Disease

    • Polymorphism, Restriction Fragment Length

    • Genotype

    • Genetic Heterogeneity

  • Genes & Molecular Sequences

    • Genome, Human

    • Alleles

    • Single Nucleotide Polymorphism

    • Dominant Genes

  • Living Beings

    • Muridae

  • Concepts & Ideas

    • Lod Score

    • Pedigree

    • Age of Onset

    • Gene Frequency

    • Linkage Disequilibrium

  • Occupations

    • Molecular Biology

  • Phenomena

    • Blotting, Southern