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  • Chromosomes, Human, Pair 7

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  • Disorders

    • Autistic Disorder

    • Genetic Markers

    • Central Nervous System Cavernous Hemangioma

    • Alcoholism

    • Charcot-Marie-Tooth Disease

    • Language Disorders

    • Hereditary Sensory and Motor Neuropathy

    • Neural Tube Defects

    • Child Development Disorders, Pervasive

    • Cavernous Hemangioma

    • Intracranial Arteriovenous Malformations

  • Chemicals & Drugs

    • Muscarinic M2 Receptors

    • Microsatellite Repeats

    • Wnt2 Protein

  • Procedures

    • Chromosome Mapping

    • Genome Wide Association Studies

    • Genetic Testing

    • Fluorescence In Situ Hybridization

    • Case Control Studies

  • Anatomy

    • Chromosomes

    • Chromosomes, Human, Pair 19

    • Chromosomes, Human, Pair 2

    • Chromosomes, Human, Pair 13

    • Chromosomes, Human, Pair 15

    • Human Chromosomes

    • Chromosomes, Human, Pair 3

    • Chromosomes, Human, Pair 6

    • Chromosomes, Human, Pair 9

    • Chromosomes, Human, Pair 4

    • Chromosomes, Human, Pair 11

    • Chromosomes, Human, Pair 8

  • Physiology

    • Genetic Predisposition to Disease

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    • DNA Copy Number Variations

  • Genes & Molecular Sequences

    • Single Nucleotide Polymorphism

    • Genome, Human

    • Dominant Genes

    • Quantitative Trait Loci

    • Alleles

  • Living Beings

    • Amish

    • European Continental Ancestry Group

  • Concepts & Ideas

    • Lod Score

    • Pedigree

    • Linkage Disequilibrium

    • Family Health

    • Gene Frequency

  • Activities & Behaviors

    • Family

  • Organizations

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