Loci identical homozygote. Medical search. Frequent questions

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Anatomy21

Chromosomes, Mammalian Chromosomes X Chromosome Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 2 Embryo, Mammalian Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 10 Cell Line Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 4 Liver Cells, Cultured Chromosomes, Human, Pair 17 Brain Chromosomes, Artificial, Yeast

Organisms12

Mice, Mutant Strains Drosophila melanogaster Mice, Inbred C57BL Mice, Inbred Strains Mice, Congenic Mice, Transgenic Mice, Knockout Mice, Neurologic Mutants Mice, Inbred C3H Arabidopsis Shrews Animals, Congenic

Diseases31

Genetic Predisposition to Disease Hemochromatosis Albinism Hyperlipoproteinemia Type II Ataxia Telangiectasia Hyperlipoproteinemia Type III Thalassemia Gaucher Disease Xanthomatosis alpha 1-Antitrypsin Deficiency Disease Susceptibility Embryo Loss alpha-Thalassemia Chromosome Inversion Cystic Fibrosis Polydactyly Polycythemia Diabetes Mellitus, Type 2 Hypolipoproteinemias Abnormalities, Multiple Syndrome Disease Models, Animal Familial Mediterranean Fever Gilbert Disease Hemoglobinopathies Neural Tube Defects Metabolism, Inborn Errors Dwarfism Fetal Death Lipid Metabolism, Inborn Errors Limb Deformities, Congenital

Chemicals and Drugs61

Genetic Markers Apolipoprotein E2 DNA DNA Primers Catechol O-Methyltransferase Methylenetetrahydrofolate Reductase (NADPH2)Membrane Proteins Ethylnitrosourea Globins Histocompatibility Antigens Class I DNA Transposable Elements RNA, Messenger Apolipoproteins E Transcription Factors DNA-Binding Proteins Ferritins Hemoglobins, Abnormal Apolipoproteins A Hemoglobin E Oxidoreductases Acting on CH-NH Group Donors Carrier Proteins HLA Antigens Codon Valine Proteins Serotonin Plasma Membrane Transport Proteins Deoxyribonucleases, Type II Site-Specific Peptidyl-Dipeptidase A Transferrin DNA, Plant Apolipoprotein C-III Iron Apolipoprotein E4 Cholesterol Fetal Hemoglobin Homeodomain Proteins Lipoproteins Cholesterol, HDL Apolipoproteins B Aryl Hydrocarbon Hydroxylases Lipids Apolipoproteins C Triglycerides Bacterial Proteins Proline Apolipoprotein A-I Homocysteine Sitosterols Drosophila Proteins Esterases DNA, Bacterial Nuclear Proteins HLA-B Antigens Cystic Fibrosis Transmembrane Conductance Regulator MNSs Blood-Group System Cholesterol Ester Transfer Proteins Repressor Proteins Folic Acid Apolipoprotein E3 Nerve Tissue Proteins Codon, Nonsense

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Chromosome Mapping Crosses, Genetic Pedigree Models, Genetic Polymerase Chain Reaction Case-Control Studies Heterozygote Detection Sequence Analysis, DNA Genome-Wide Association Study Genetic Association Studies DNA Mutational Analysis Genetic Testing Risk Factors Blotting, Southern Inbreeding Cloning, Molecular Mutagenesis, Insertional Amino Acid Substitution Restriction Mapping Genetic Complementation Test Cohort Studies Genotyping Techniques Pigmentation Gene Targeting Odds Ratio Reference Values Sequence Alignment Risk Physical Chromosome Mapping Analysis of Variance Nucleic Acid Hybridization Likelihood Functions Gene Knock-In Techniques Reverse Transcriptase Polymerase Chain Reaction Disease Models, Animal Electrophoresis, Starch Gel Hybridization, Genetic

Psychiatry and Psychology1

Phenomena and Processes105

Homozygote Genetic Loci Genotype Heterozygote Polymorphism, Genetic Quantitative Trait Loci Gene Frequency Alleles Genetic Predisposition to Disease Polymorphism, Single Nucleotide Phenotype Mutation Genetic Linkage Genetic Variation Genetic Markers Base Sequence Microsatellite Repeats Linkage Disequilibrium Polymorphism, Restriction Fragment Length Haplotypes Lod Score Genes, Dominant Genes, Lethal Recombination, Genetic Genes Exons Genes, Recessive Amino Acid Sequence Point Mutation Quantitative Trait, Heritable Promoter Regions, Genetic Selection, Genetic Chromosomes, Mammalian Chromosomes Hair Color Genetic Heterogeneity Inbreeding Mutation, Missense Multigene Family Mutagenesis, Insertional Amino Acid Substitution Minisatellite Repeats Species Specificity Genome, Human Phylogeny Genes, Plant Penetrance Consanguinity DNA Transposable Elements Introns Transcription, Genetic X Chromosome Gene Expression Regulation Evolution, Molecular Pigmentation Sequence Deletion Chromosomes, Human, Pair 9 Gene Dosage Gene Expression Odds Ratio Genes, Bacterial Chromosomes, Human, Pair 1 Diploidy Gene Expression Regulation, Developmental Codon Chromosomes, Human, Pair 2 Genes, Insect Founder Effect Disease Susceptibility Major Histocompatibility Complex Sequence Homology, Amino Acid Genes, Mating Type, Fungal Polymorphism, Single-Stranded Conformational Risk Haploidy Mutagenesis Genes, Regulator Eye Color Biological Evolution Nucleic Acid Hybridization Chromosome Inversion Chromosomes, Human, Pair 16 Genome Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 19 Sequence Homology, Nucleic Acid Chromosomes, Human, Pair 7 Genetic Load Chromosomes, Human, Pair 12 Gene Deletion Frameshift Mutation Reproduction Chromosomes, Human, Pair 10 Hybrid Vigor Chromosomes, Human, Pair 5 Embryonic and Fetal Development Time Factors Crossing Over, Genetic Chromosomes, Human, Pair 4 Hybridization, Genetic Chromosomes, Human, Pair 17 Genomic Imprinting Genome, Plant Codon, Nonsense Chromosomes, Artificial, Yeast

Disciplines and Occupations1

Genetics, Population

Anthropology, Education, Sociology and Social Phenomena1

Information Science5

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny Publication Bias

Named Groups6

Asian Continental Ancestry Group European Continental Ancestry Group Jews Ethnic Groups African Continental Ancestry Group Siblings

Health Care13

Case-Control Studies Genome-Wide Association Study Genetic Testing Risk Factors Cohort Studies Age of Onset Odds Ratio Family Health Ethnic Groups Risk Analysis of Variance Likelihood Functions Sex Factors

Geographicals4

China Czech Republic Japan Italy

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care Geographicals

Homozygote Genetic Loci Genotype Heterozygote Polymorphism, Genetic Quantitative Trait Loci Chromosome Mapping Gene Frequency Alleles Genetic Predisposition to Disease Polymorphism, Single Nucleotide Phenotype Mutation Genetic Linkage Genetic Variation Genetic Markers Crosses, Genetic Hemochromatosis Base Sequence Molecular Sequence Data Pedigree Microsatellite Repeats Models, Genetic Polymerase Chain Reaction Linkage Disequilibrium Case-Control Studies Heterozygote Detection Polymorphism, Restriction Fragment Length Haplotypes Mice, Mutant Strains Lod Score Genes, Dominant Genetics, Population Sequence Analysis, DNA Genome-Wide Association Study Genes, Lethal Genetic Association Studies Albinism Recombination, Genetic Genes Apolipoprotein E2 Exons DNA DNA Primers Genes, Recessive Amino Acid Sequence Catechol O-Methyltransferase Asian Continental Ancestry Group European Continental Ancestry Group Point Mutation Hyperlipoproteinemia Type II DNA Mutational Analysis Genetic Testing Quantitative Trait, Heritable Methylenetetrahydrofolate Reductase (NADPH2)Promoter Regions, Genetic Risk Factors Selection, Genetic Drosophila melanogaster Chromosomes, Mammalian Chromosomes Hair Color Blotting, Southern Genetic Heterogeneity Inbreeding Mutation, Missense Cloning, Molecular Membrane Proteins Mice, Inbred C57BL Multigene Family Mutagenesis, Insertional Amino Acid Substitution Ethylnitrosourea Minisatellite Repeats Species Specificity Genome, Human Phylogeny Genes, Plant Restriction Mapping Globins Penetrance Histocompatibility Antigens Class I Genetic Complementation Test Ataxia Telangiectasia Consanguinity DNA Transposable Elements Introns Cohort Studies RNA, Messenger Apolipoproteins E Transcription, Genetic X Chromosome Transcription Factors Jews Gene Expression Regulation Genotyping Techniques Mice, Inbred Strains Evolution, Molecular DNA-Binding Proteins Hyperlipoproteinemia Type III

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