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Anatomy18

Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 5 X Chromosome Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 9 Chromosomes, Human, X Chromosomes, Human, Pair 11

Organisms3

Larix Pinus taeda Animals, Domestic

Diseases17

Genetic Predisposition to Disease Hip Dysplasia, Canine Optic Atrophy, Hereditary, Leber Genetic Diseases, Inborn Syndrome Optic Atrophies, Hereditary Retinitis Pigmentosa Corneal Dystrophies, Hereditary Anticipation, Genetic Diseases in Twins Duane Retraction Syndrome Brachial Plexus Neuritis Malignant Hyperthermia Sex Chromosome Aberrations Prosthesis Failure Cataract Muscular Dystrophies

Chemicals and Drugs3

Genetic Markers DNA, Mitochondrial Eye Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Pedigree Registries Models, Genetic Chromosome Mapping Inbreeding Breeding Likelihood Functions DNA Mutational Analysis Genetic Testing Risk Factors Randomized Controlled Trials as Topic Cohort Studies Heterozygote Detection Incidence Probability Models, Statistical Markov Chains Monte Carlo Method Research Design Genome-Wide Association Study Follow-Up Studies Treatment Outcome Equipment Safety Case-Control Studies Sequence Analysis, DNA Bayes Theorem Risk Crosses, Genetic Prevalence Polymerase Chain Reaction Reproducibility of Results Questionnaires Records as Topic Regression Analysis Device Approval Medical Records Prosthesis Failure Data Interpretation, Statistical Prospective Studies Retrospective Studies Risk Assessment Cause of Death

Psychiatry and Psychology7

Nuclear Family Family Siblings Adult Children Bipolar Disorder Schizophrenia Schizophrenia, Catatonic

Phenomena and Processes66

Genetic Linkage Lod Score Genetic Markers Genes, Dominant Genotype Haplotypes Phenotype Consanguinity Inbreeding Microsatellite Repeats Inheritance Patterns Alleles Breeding Quantitative Trait Loci Penetrance Genetic Predisposition to Disease Quantitative Trait, Heritable Genes, Recessive Mutation Heterozygote Linkage Disequilibrium Founder Effect Polymorphism, Single Nucleotide Chromosomes, Human, Pair 1 Genetic Variation Genome, Human Algorithms Multifactorial Inheritance Genetic Heterogeneity Chromosomes, Human, Pair 2 Gene Frequency Probability Homozygote Markov Chains Heredity Base Sequence Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 5 X Chromosome Chromosomes, Human, Pair 10 Exons Pregnancy Mutation, Missense Polymorphism, Genetic Chromosomes, Human, Pair 7 Time Factors Point Mutation Chromosomes, Human, Pair 20 Polymorphism, Restriction Fragment Length Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 12 Genetic Loci Risk Exome Chromosomes, Human, Pair 17 Anticipation, Genetic Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 9 Recombination, Genetic Polymorphism, Single-Stranded Conformational Sex Chromosome Aberrations Chromosomes, Human, X Chromosomes, Human, Pair 11

Disciplines and Occupations3

Genetics, Population Genetics, Medical Research Design

Anthropology, Education, Sociology and Social Phenomena7

Nuclear Family Family Paternity Siblings Adult Children Age Distribution United States Food and Drug Administration

Humanities1

Genealogy and Heraldry

Information Science15

Registries Computer Simulation Algorithms Software Incidence Monte Carlo Method Molecular Sequence Data Base Sequence Prevalence Questionnaires Records as Topic Databases, Factual Medical Records Data Interpretation, Statistical Cause of Death

Named Groups5

Siblings Amish Infant, Newborn Asian Continental Ancestry Group Adult Children

Health Care36

Registries Family Health Likelihood Functions Age of Onset Genetic Testing Risk Factors Randomized Controlled Trials as Topic Cohort Studies Incidence Probability Models, Statistical Markov Chains Monte Carlo Method Sex Factors Age Factors Genome-Wide Association Study Follow-Up Studies Treatment Outcome Case-Control Studies Age Distribution Bayes Theorem Risk Prevalence Pensions Reproducibility of Results Questionnaires Records as Topic United States Food and Drug Administration Regression Analysis Device Approval Medical Records Data Interpretation, Statistical Prospective Studies Retrospective Studies Risk Assessment Cause of Death

Geographicals15

Sweden Utah Denmark Finland Great Britain Netherlands Palau England Norway Europe London Azores China Italy Germany

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Humanities Information Science Named Groups Health Care Geographicals

Pedigree Genetic Linkage Lod Score Registries Models, Genetic Chromosome Mapping Genetic Markers Sweden Genes, Dominant Genotype Haplotypes Utah Phenotype Consanguinity Inbreeding Microsatellite Repeats Inheritance Patterns Family Health Denmark Alleles Breeding Quantitative Trait Loci Penetrance Finland Genetic Predisposition to Disease Quantitative Trait, Heritable Likelihood Functions Genes, Recessive Mutation Heterozygote Linkage Disequilibrium Nuclear Family Founder Effect DNA Mutational Analysis Computer Simulation Polymorphism, Single Nucleotide Genealogy and Heraldry Age of Onset Family Chromosomes, Human, Pair 1 Hip Dysplasia, Canine Genetic Testing Genetic Variation Genome, Human Algorithms Risk Factors Multifactorial Inheritance Randomized Controlled Trials as Topic Paternity Genetic Heterogeneity Cohort Studies Optic Atrophy, Hereditary, Leber Heterozygote Detection Software Siblings Genetics, Population Incidence Chromosomes, Human, Pair 2 Gene Frequency Genetic Diseases, Inborn Probability Great Britain Amish Homozygote Netherlands Models, Statistical Palau Markov Chains Monte Carlo Method Genetics, Medical Heredity Molecular Sequence Data England Research Design Infant, Newborn Base Sequence Sex Factors Chromosomes, Human, Pair 19 Age Factors Chromosomes, Human, Pair 3 Syndrome Norway Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 5 X Chromosome Chromosomes, Human, Pair 10 Exons Asian Continental Ancestry Group Pregnancy Optic Atrophies, Hereditary Mutation, Missense Genome-Wide Association Study DNA, Mitochondrial Polymorphism, Genetic Chromosomes, Human, Pair 7 Follow-Up Studies Treatment Outcome Time Factors Retinitis Pigmentosa Point Mutation

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