Genotypes heterozygote. Medical search. Frequent questions

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Anatomy9

X Chromosome Fibroblasts Chromosomes Sex Chromosomes Erythrocytes Hair Liver Cells, Cultured Leukocytes

Organisms12

Hepacivirus Mice, Mutant Strains Mice, Knockout Mice, Inbred C57BL Shrews Hepatitis B virus Drosophila melanogaster Mice, Inbred Strains Chimera Mice, Transgenic Hepatitis E virus Cattle

Diseases48

Genetic Predisposition to Disease Thalassemia Hyperlipoproteinemia Type I Hemochromatosis Ataxia Telangiectasia Hyperlipoproteinemia Type II Cystinuria Hypobetalipoproteinemias Tay-Sachs Disease alpha-Thalassemia Hemoglobinopathies beta-Thalassemia Hepatitis C Phenylketonurias Hepatitis C, Chronic Glucosephosphate Dehydrogenase Deficiency Cystic Fibrosis Sandhoff Disease Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Metabolism, Inborn Errors Disease Susceptibility Fabry Disease alpha 1-Antitrypsin Deficiency Homocystinuria Hypolipoproteinemias Lipidoses Albinism Lecithin Acyltransferase Deficiency Chromosome Inversion Familial Mediterranean Fever Syndrome Lesch-Nyhan Syndrome Purine-Pyrimidine Metabolism, Inborn Errors Iron Overload Hyperlipoproteinemias Adrenal Hyperplasia, Congenital Gaucher Disease Dwarfism Chromosome Deletion Xanthomatosis Sex Chromosome Aberrations Disease Progression Hepatitis B Disease Models, Animal Sickle Cell Trait Anemia, Sickle Cell Tangier Disease

Chemicals and Drugs57

Genetic Markers Hemoglobin A2 Methylenetetrahydrofolate Reductase (NADPH2)Hemoglobins, Abnormal DNA Primers Hemoglobin E DNA Adenine Phosphoribosyltransferase Catechol O-Methyltransferase Apolipoproteins E Fetal Hemoglobin Glutathione Transferase Peptidyl-Dipeptidase A Apolipoprotein E4 RNA, Viral Aryl Hydrocarbon Hydroxylases Ribavirin Globins Arylamine N-Acetyltransferase Codon, Nonsense Codon Antiviral Agents Serotonin Plasma Membrane Transport Proteins Apolipoproteins B DNA, Viral Lipoprotein Lipase Hexosaminidase A Oxidoreductases Acting on CH-NH Group Donors Factor V Membrane Proteins HLA Antigens Hemoglobin, Sickle Interferon-alpha RNA, Messenger Apolipoprotein B-100 Ethylnitrosourea Glucosephosphate Dehydrogenase Isoenzymes beta-N-Acetylhexosaminidases Apolipoprotein E2 Polyethylene Glycols Lipids Cystic Fibrosis Transmembrane Conductance Regulator Homocysteine Carrier Proteins 2-Aminopurine Cholesterol, HDL DNA-Binding Proteins Cholesterol Cytochrome P-450 CYP2D6 Glutathione S-Transferase pi Ferritins Lipoproteins Apolipoprotein A-I alpha 1-Antitrypsin Iron Viral Nonstructural Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Heterozygote Detection Pedigree Polymerase Chain Reaction Case-Control Studies Sequence Analysis, DNA DNA Mutational Analysis Crosses, Genetic Models, Genetic Risk Factors Chromosome Mapping Genetic Testing Genotyping Techniques Inbreeding Molecular Epidemiology Amino Acid Substitution Cohort Studies Odds Ratio Breeding Cluster Analysis Electrophoresis, Starch Gel Prevalence Hybridization, Genetic Reverse Transcriptase Polymerase Chain Reaction Risk Genome-Wide Association Study Reference Values Analysis of Variance Likelihood Functions Heteroduplex Analysis DNA Fingerprinting Prospective Studies Viral Load Chi-Square Distribution Blotting, Southern Gene Targeting Prenatal Diagnosis Sensitivity and Specificity Logistic Models Molecular Typing Disease Models, Animal Sequence Alignment Genetic Complementation Test

Psychiatry and Psychology1

Phenomena and Processes81

Heterozygote Genotype Homozygote Polymorphism, Genetic Alleles Gene Frequency Mutation Phenotype Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genetic Variation Haplotypes Polymorphism, Restriction Fragment Length Base Sequence Genetic Markers Phylogeny Genes, Recessive Point Mutation Genes, Dominant Mutation, Missense Genetic Linkage Exons Linkage Disequilibrium Microsatellite Repeats Genes, Lethal Inbreeding Selection, Genetic Amino Acid Substitution Gene Deletion Amino Acid Sequence Recombination, Genetic Odds Ratio Minisatellite Repeats Hybrid Vigor Epistasis, Genetic Frameshift Mutation Breeding Polymorphism, Single-Stranded Conformational Codon, Nonsense Codon Sequence Deletion Consanguinity Hybridization, Genetic Promoter Regions, Genetic Gene Dosage Introns Disease Susceptibility Genes Quantitative Trait Loci Diploidy Haploidy Pregnancy Crossing Over, Genetic Penetrance Hair Color Risk Species Specificity Founder Effect Time Factors X Chromosome Genetic Heterogeneity Chromosome Inversion Chromosomes Genome, Viral Quantitative Trait, Heritable Inheritance Patterns Evolution, Molecular Sex Chromosomes Genetic Loci Reproduction Sex Characteristics Environment Fertility Hemizygote Chromosome Deletion Sex Chromosome Aberrations Viral Load Chi-Square Distribution Sensitivity and Specificity Gene Expression Gene-Environment Interaction

Disciplines and Occupations4

Genetics, Population Molecular Epidemiology Pharmacogenetics Geography

Anthropology, Education, Sociology and Social Phenomena1

DNA Fingerprinting

Technology, Industry, Agriculture1

Polyethylene Glycols

Information Science5

Molecular Sequence Data Base Sequence Phylogeny Amino Acid Sequence Prevalence

Named Groups6

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

Health Care22

Case-Control Studies Risk Factors Genetic Testing Molecular Epidemiology Cohort Studies Odds Ratio Age of Onset Cluster Analysis Prevalence Risk Family Health Genome-Wide Association Study Ethnic Groups Analysis of Variance Sex Factors Likelihood Functions Environment Age Factors Prospective Studies Chi-Square Distribution Sensitivity and Specificity Logistic Models

Geographicals8

China Japan Italy Brazil Korea Czech Republic France Turkey

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

Heterozygote Genotype Heterozygote Detection Homozygote Polymorphism, Genetic Alleles Gene Frequency Mutation Phenotype Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genetic Variation Pedigree Polymerase Chain Reaction Haplotypes Molecular Sequence Data Polymorphism, Restriction Fragment Length Case-Control Studies Base Sequence Sequence Analysis, DNA DNA Mutational Analysis Thalassemia Genetic Markers Crosses, Genetic Models, Genetic Phylogeny Genes, Recessive Asian Continental Ancestry Group Hemoglobin A2 Point Mutation Hyperlipoproteinemia Type I Genes, Dominant Mutation, Missense Genetic Linkage Genetics, Population Exons Hemochromatosis Linkage Disequilibrium Risk Factors Microsatellite Repeats Chromosome Mapping Genes, Lethal Genetic Testing Hepacivirus Methylenetetrahydrofolate Reductase (NADPH2)Genotyping Techniques Hemoglobins, Abnormal China DNA Primers Ataxia Telangiectasia Hyperlipoproteinemia Type II Mice, Mutant Strains Hemoglobin E DNA Jews Inbreeding Cystinuria Hypobetalipoproteinemias Selection, Genetic Tay-Sachs Disease alpha-Thalassemia Mice, Knockout Adenine Phosphoribosyltransferase Catechol O-Methyltransferase Molecular Epidemiology Apolipoproteins E European Continental Ancestry Group Amino Acid Substitution Gene Deletion Fetal Hemoglobin Glutathione Transferase Amino Acid Sequence Japan Cohort Studies Peptidyl-Dipeptidase A Mice, Inbred C57BL Hemoglobinopathies beta-Thalassemia Recombination, Genetic Odds Ratio Hepatitis C Phenylketonurias Apolipoprotein E4 Hepatitis C, Chronic Glucosephosphate Dehydrogenase Deficiency Minisatellite Repeats Italy Cystic Fibrosis RNA, Viral Shrews Hybrid Vigor Aryl Hydrocarbon Hydroxylases Epistasis, Genetic Sandhoff Disease Frameshift Mutation Age of Onset Amino Acid Metabolism, Inborn Errors Ribavirin Hepatitis B virus Globins

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