Loci heterozygote homozygote. Medical search. Frequent questions

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Anatomy12

Chromosomes Chromosomes, Mammalian X Chromosome Fibroblasts Embryo, Mammalian Hair Cells, Cultured Erythrocytes Chromosomes, Human, Pair 1 Liver Lymphocytes Cell Line

Organisms10

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

Diseases46

Genetic Predisposition to Disease Hemochromatosis Thalassemia Hyperlipoproteinemia Type II Ataxia Telangiectasia Albinism Hyperlipoproteinemia Type I alpha-Thalassemia Hypobetalipoproteinemias Hemoglobinopathies alpha 1-Antitrypsin Deficiency Xanthomatosis Hypolipoproteinemias Cystinuria Tay-Sachs Disease Metabolism, Inborn Errors Cystic Fibrosis beta-Thalassemia Lipid Metabolism, Inborn Errors Chromosome Inversion Gaucher Disease Glucosephosphate Dehydrogenase Deficiency Lecithin Acyltransferase Deficiency Familial Mediterranean Fever Hyperlipoproteinemia Type III Syndrome Homocystinuria Dwarfism Disease Susceptibility Embryo Loss Polycythemia Abnormalities, Multiple Fetal Death Neural Tube Defects Hyperlipoproteinemias Amino Acid Metabolism, Inborn Errors Tangier Disease Sandhoff Disease Disease Models, Animal Polydactyly Eye Abnormalities Gilbert Disease Phenylketonurias Retinal Degeneration Chromosome Deletion Chromosome Aberrations

Chemicals and Drugs62

Genetic Markers DNA Hemoglobins, Abnormal DNA Primers Hemoglobin E Globins Hemoglobin A2 Fetal Hemoglobin Apolipoprotein E2 Methylenetetrahydrofolate Reductase (NADPH2)Ethylnitrosourea Membrane Proteins Catechol O-Methyltransferase Adenine Phosphoribosyltransferase RNA, Messenger Histocompatibility Antigens Class I Apolipoproteins E Apolipoproteins B Ferritins Codon, Nonsense HLA Antigens DNA-Binding Proteins Codon Transcription Factors Apolipoproteins A Carrier Proteins Lipoprotein Lipase DNA Transposable Elements Iron Factor V Cholesterol Lipoproteins Proteins Oxidoreductases Acting on CH-NH Group Donors Apolipoprotein E4 Apolipoprotein A-I Cystic Fibrosis Transmembrane Conductance Regulator Cholesterol, HDL Hemoglobin, Sickle Transferrin Sitosterols Lipids Apolipoprotein B-100 alpha 1-Antitrypsin Receptors, LDL Triglycerides beta-N-Acetylhexosaminidases Homeodomain Proteins Valine MNSs Blood-Group System Isoenzymes Arginine Lipoproteins, LDL Apolipoprotein C-III Aryl Hydrocarbon Hydroxylases Deoxyribonucleases, Type II Site-Specific Peptidyl-Dipeptidase A Apolipoproteins Serotonin Plasma Membrane Transport Proteins Lipoproteins, HDL Hexosaminidase B Hexosaminidases

Analytical, Diagnostic and Therapeutic Techniques and Equipment38

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

Phenomena and Processes90

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

Disciplines and Occupations1

Genetics, Population

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups6

Jews Asian Continental Ancestry Group European Continental Ancestry Group African Continental Ancestry Group Ethnic Groups Infant, Newborn

Health Care13

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

Geographicals4

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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 Heterozygote Heterozygote Detection Genotype Genetic Loci Polymorphism, Genetic Alleles Mutation Phenotype Gene Frequency Pedigree Quantitative Trait Loci Chromosome Mapping Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genetic Variation Genetic Linkage Crosses, Genetic Base Sequence Hemochromatosis Genetic Markers Molecular Sequence Data Polymerase Chain Reaction Microsatellite Repeats Models, Genetic Genes, Dominant Genes, Recessive Haplotypes Genes, Lethal Polymorphism, Restriction Fragment Length Mice, Mutant Strains DNA Mutational Analysis Case-Control Studies Thalassemia Point Mutation Exons Hyperlipoproteinemia Type II Linkage Disequilibrium Genetics, Population Mutation, Missense Genetic Testing Ataxia Telangiectasia DNA Sequence Analysis, DNA Hemoglobins, Abnormal Albinism Genes Hyperlipoproteinemia Type I Jews DNA Primers Recombination, Genetic Hemoglobin E Inbreeding Selection, Genetic Genetic Association Studies Amino Acid Sequence Lod Score Asian Continental Ancestry Group Globins Mice, Inbred C57BL Hemoglobin A2 Genome-Wide Association Study Fetal Hemoglobin European Continental Ancestry Group Drosophila melanogaster Chromosomes Hair Color Risk Factors Apolipoprotein E2 alpha-Thalassemia Hypobetalipoproteinemias Mice, Knockout Methylenetetrahydrofolate Reductase (NADPH2)Consanguinity Ethylnitrosourea Membrane Proteins Catechol O-Methyltransferase Amino Acid Substitution Blotting, Southern Promoter Regions, Genetic Hemoglobinopathies Genetic Heterogeneity Sequence Deletion Chromosomes, Mammalian X Chromosome Quantitative Trait, Heritable Introns Shrews Penetrance alpha 1-Antitrypsin Deficiency Frameshift Mutation Adenine Phosphoribosyltransferase RNA, Messenger Genetic Complementation Test Xanthomatosis Diploidy Hypolipoproteinemias Gene Dosage Gene Targeting Cystinuria

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