Produce heterozygote homozygote. Medical search. Frequent questions

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Anatomy14

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

Organisms11

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

Diseases50

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 Tay-Sachs Disease Cystinuria Metabolism, Inborn Errors beta-Thalassemia Lipid Metabolism, Inborn Errors Cystic Fibrosis Glucosephosphate Dehydrogenase Deficiency Gaucher Disease Lecithin Acyltransferase Deficiency Hyperlipoproteinemia Type III Familial Mediterranean Fever Homocystinuria Chromosome Inversion Embryo Loss Polycythemia Disease Models, Animal Dwarfism Sandhoff Disease Tangier Disease Hyperlipoproteinemias Neural Tube Defects Fetal Death Amino Acid Metabolism, Inborn Errors Phenylketonurias Chromosome Deletion Gilbert Disease Disease Susceptibility Syndrome Polydactyly Eye Abnormalities Abnormalities, Multiple Abetalipoproteinemia Retinal Degeneration Fabry Disease Anemia, Sickle Cell Lipidoses Lesch-Nyhan Syndrome

Chemicals and Drugs70

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

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

Phenomena and Processes74

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 Exons Mutation, Missense Polymorphism, Restriction Fragment Length Genetic Linkage Genetic Markers Amino Acid Sequence Linkage Disequilibrium Amino Acid Substitution Inbreeding Gene Deletion Genes Selection, Genetic Hair Color Microsatellite Repeats Frameshift Mutation Sequence Deletion Codon, Nonsense Consanguinity Hybrid Vigor Chromosomes Promoter Regions, Genetic Codon Time Factors Introns Recombination, Genetic Diploidy Penetrance Chromosome Inversion Founder Effect Polymorphism, Single-Stranded Conformational Gene Expression Haploidy Gene Dosage Crossing Over, Genetic Odds Ratio Gene Expression Regulation, Developmental Pregnancy Epistasis, Genetic Eye Color Chromosome Deletion Disease Susceptibility Genetic Load Pigmentation Risk Gene Expression Regulation Genetic Heterogeneity Mutagenesis, Insertional X Chromosome Embryonic and Fetal Development Kinetics Meiosis Fertility Reproduction Major Histocompatibility Complex Mutagenesis Species Specificity Chromosomes, Mammalian

Disciplines and Occupations1

Genetics, Population

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Publication Bias

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

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

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