Heterozygotes identical homozygote. Medical search. Frequent questions

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Anatomy12

Chromosomes Fibroblasts Embryo, Mammalian Hair Erythrocytes X Chromosome Cells, Cultured Lymphocytes Liver Leukocytes Chromosomes, Mammalian Brain

Organisms10

Mice, Mutant Strains Mice, Knockout Shrews Mice, Inbred C57BL Drosophila melanogaster Mice, Neurologic Mutants Mice, Transgenic Mice, Inbred Strains Rats, Mutant Strains Chimera

Diseases53

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

Chemicals and Drugs73

Hemoglobins, Abnormal Hemoglobin E Genetic Markers Hemoglobin A2 Apolipoprotein E2 Methylenetetrahydrofolate Reductase (NADPH2)DNA Fetal Hemoglobin Catechol O-Methyltransferase Ethylnitrosourea DNA Primers Globins Membrane Proteins Ferritins Histocompatibility Antigens Class I Apolipoproteins B Apolipoproteins E Adenine Phosphoribosyltransferase Codon, Nonsense Apolipoproteins A Lipoprotein Lipase Codon Factor V Cholesterol Iron Oxidoreductases Acting on CH-NH Group Donors Apolipoprotein E4 Apolipoprotein A-I HLA Antigens Cystic Fibrosis Transmembrane Conductance Regulator Lipoproteins RNA, Messenger Transferrin Hemoglobin, Sickle Apolipoprotein B-100 Sitosterols alpha 1-Antitrypsin Cholesterol, HDL beta-N-Acetylhexosaminidases Lipids Receptors, LDL Carrier Proteins Triglycerides Lipoproteins, LDL MNSs Blood-Group System Valine Hexosaminidase B Arginine Serotonin Plasma Membrane Transport Proteins Apolipoprotein C-III Lipoproteins, HDL Hexosaminidases DNA-Binding Proteins Aryl Hydrocarbon Hydroxylases Apolipoproteins Peptidyl-Dipeptidase A Homocysteine Cholesterol Ester Transfer Proteins Hexosaminidase A Prothrombin Proline Proteins Eye Proteins Phosphatidylcholine-Sterol O-Acyltransferase Apolipoproteins C Isoenzymes Lipase Transcription Factors Glucosylceramidase Deoxyribonucleases, Type II Site-Specific 2-Aminopurine Folic Acid Cystathionine beta-Synthase

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

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

Phenomena and Processes72

Homozygote Heterozygote Genotype Alleles Polymorphism, Genetic Mutation Gene Frequency Phenotype Genetic Predisposition to Disease Polymorphism, Single Nucleotide Genetic Variation Genes, Recessive Haplotypes Genes, Lethal Base Sequence Point Mutation Genes, Dominant Mutation, Missense Exons Polymorphism, Restriction Fragment Length Genetic Linkage Genetic Markers Linkage Disequilibrium Inbreeding Amino Acid Substitution Hair Color Selection, Genetic Microsatellite Repeats Gene Deletion Genes Frameshift Mutation Consanguinity Codon, Nonsense Hybrid Vigor Amino Acid Sequence Sequence Deletion Chromosomes Codon Penetrance Founder Effect Chromosome Inversion Introns Polymorphism, Single-Stranded Conformational Promoter Regions, Genetic Odds Ratio Diploidy Crossing Over, Genetic Gene Dosage Haploidy Recombination, Genetic Epistasis, Genetic Eye Color Genetic Load Risk Gene Expression Regulation, Developmental Genetic Heterogeneity Chromosome Deletion Disease Susceptibility Pregnancy X Chromosome Pigmentation Embryonic and Fetal Development Gene Expression Major Histocompatibility Complex Meiosis Mutagenesis, Insertional Fertility Chromosomes, Mammalian Minisatellite Repeats Nondisjunction, Genetic Time Factors Gene Expression Regulation

Disciplines and Occupations1

Genetics, Population

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Publication Bias

Named Groups7

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

Health Care11

Case-Control Studies Genetic Testing Risk Factors Age of Onset Cohort Studies Odds Ratio Family Health Ethnic Groups Risk Analysis of Variance Sex Factors

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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 Alleles Polymorphism, Genetic Mutation Gene Frequency Phenotype Pedigree Genetic Predisposition to Disease Hemochromatosis Polymorphism, Single Nucleotide Genetic Variation Genes, Recessive Haplotypes Genes, Lethal Thalassemia Crosses, Genetic Polymerase Chain Reaction Hyperlipoproteinemia Type II Mice, Mutant Strains Base Sequence Point Mutation Case-Control Studies Genes, Dominant DNA Mutational Analysis Ataxia Telangiectasia Molecular Sequence Data Mutation, Missense Hemoglobins, Abnormal Exons Hyperlipoproteinemia Type I Polymorphism, Restriction Fragment Length Genetic Testing Hemoglobin E Genetic Linkage Albinism Jews Models, Genetic Chromosome Mapping Genetic Markers Hemoglobin A2 Apolipoprotein E2 Hypobetalipoproteinemias alpha-Thalassemia Genetics, Population Methylenetetrahydrofolate Reductase (NADPH2)DNA Asian Continental Ancestry Group Fetal Hemoglobin Linkage Disequilibrium Catechol O-Methyltransferase Genetic Association Studies Risk Factors Inbreeding Hemoglobinopathies Amino Acid Substitution Mice, Knockout Ethylnitrosourea Shrews alpha 1-Antitrypsin Deficiency Xanthomatosis Hair Color DNA Primers Hypolipoproteinemias Cystinuria Selection, Genetic Globins Microsatellite Repeats Gene Deletion Tay-Sachs Disease European Continental Ancestry Group Membrane Proteins Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Genes Ferritins beta-Thalassemia Frameshift Mutation Mice, Inbred C57BL Histocompatibility Antigens Class I Cystic Fibrosis Apolipoproteins B Glucosephosphate Dehydrogenase Deficiency Gaucher Disease Electrophoresis, Starch Gel Apolipoproteins E Adenine Phosphoribosyltransferase Lecithin Acyltransferase Deficiency Consanguinity Sequence Analysis, DNA Codon, Nonsense Hybrid Vigor Drosophila melanogaster Hyperlipoproteinemia Type III Apolipoproteins A Familial Mediterranean Fever Amino Acid Sequence Sequence Deletion

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