Possess heterozygote. Medical search. Frequent questions

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Anatomy11

Fibroblasts Chromosomes X Chromosome Hair Erythrocytes Sex Chromosomes Leukocytes Cells, Cultured Lymphocytes Sweat Embryo, Mammalian

Organisms8

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

Diseases57

Thalassemia Hyperlipoproteinemia Type I Hemochromatosis Ataxia Telangiectasia Genetic Predisposition to Disease Hyperlipoproteinemia Type II Cystinuria Hypobetalipoproteinemias Tay-Sachs Disease alpha-Thalassemia Hemoglobinopathies Sandhoff Disease beta-Thalassemia Glucosephosphate Dehydrogenase Deficiency Amino Acid Metabolism, Inborn Errors Phenylketonurias Lipid Metabolism, Inborn Errors Metabolism, Inborn Errors Fabry Disease Hypolipoproteinemias Homocystinuria Lipidoses Lecithin Acyltransferase Deficiency Cystic Fibrosis Lesch-Nyhan Syndrome alpha 1-Antitrypsin Deficiency Albinism Chromosome Inversion Hyperlipoproteinemias Purine-Pyrimidine Metabolism, Inborn Errors Xanthomatosis Familial Mediterranean Fever Iron Overload Dwarfism Tangier Disease Syndrome Cystinosis Adrenal Hyperplasia, Congenital Sex Chromosome Aberrations Chromosome Deletion Hyperargininemia Mucopolysaccharidosis II Ornithine Carbamoyltransferase Deficiency Disease Sickle Cell Trait Glycogen Storage Disease Type V Eye Abnormalities Embryo Loss Gaucher Disease Anemia, Sickle Cell Fetal Death Xeroderma Pigmentosum Retinitis Pigmentosa Neural Tube Defects Tyrosinemias Anemia, Hemolytic, Congenital Nonspherocytic Retinal Degeneration Elliptocytosis, Hereditary

Chemicals and Drugs45

Hemoglobin A2 Hemoglobins, Abnormal Hemoglobin E Adenine Phosphoribosyltransferase Fetal Hemoglobin DNA Genetic Markers Globins Codon, Nonsense Hexosaminidase A Apolipoproteins B DNA Primers Lipoprotein Lipase Ethylnitrosourea Apolipoprotein B-100 Hemoglobin, Sickle beta-N-Acetylhexosaminidases 2-Aminopurine Factor V Glucosephosphate Dehydrogenase Membrane Proteins HLA Antigens Cystic Fibrosis Transmembrane Conductance Regulator alpha-Galactosidase RNA, Messenger HLA-DRB3 Chains alpha 1-Antitrypsin Codon Ferritins Receptors, LDL Eye Proteins Apolipoprotein A-I Lipoproteins Iduronate Sulfatase Iron Cholesterol Sitosterols Histocompatibility Antigens Class I Isoenzymes Apolipoproteins E Cholesterol, HDL Hexosaminidases Apolipoproteins A Hemoglobin C Carrier Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Heterozygote Detection Pedigree DNA Mutational Analysis Crosses, Genetic Polymerase Chain Reaction Models, Genetic Genetic Testing Chromosome Mapping Inbreeding Case-Control Studies Electrophoresis, Starch Gel Sequence Analysis, DNA Amino Acid Substitution Gene Targeting Prenatal Diagnosis Electroretinography Risk Factors Genotyping Techniques Genetic Complementation Test Blotting, Southern Heteroduplex Analysis Hybridization, Genetic Genetic Association Studies Blood Protein Electrophoresis Reference Values

Phenomena and Processes59

Heterozygote Homozygote Alleles Genotype Mutation Phenotype Polymorphism, Genetic Gene Frequency Genes, Recessive Genetic Variation Genes, Dominant Genes, Lethal Base Sequence Genetic Predisposition to Disease Point Mutation Haplotypes Mutation, Missense Exons Genetic Linkage Polymorphism, Single Nucleotide Inbreeding Polymorphism, Restriction Fragment Length Genetic Markers Microsatellite Repeats Frameshift Mutation Selection, Genetic Codon, Nonsense Consanguinity Hybrid Vigor Gene Deletion Crossing Over, Genetic Genes Haploidy Chromosome Inversion Sequence Deletion Amino Acid Sequence Linkage Disequilibrium Polymorphism, Single-Stranded Conformational Amino Acid Substitution Hair Color Hemizygote Chromosomes Diploidy X Chromosome Founder Effect Recombination, Genetic Gene Dosage Introns Sex Chromosomes Penetrance Sex Chromosome Aberrations Chromosome Deletion Codon Pregnancy Epistasis, Genetic Hybridization, Genetic Gene Expression Regulation, Developmental Genetic Heterogeneity Genetic Load

Disciplines and Occupations1

Genetics, Population

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups5

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

Health Care6

Genetic Testing Case-Control Studies Family Health Family Leave Risk Factors Age of Onset

Geographicals2

Italy Czech Republic

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

Heterozygote Heterozygote Detection Homozygote Alleles Genotype Mutation Pedigree Phenotype Polymorphism, Genetic Gene Frequency Thalassemia Genes, Recessive Hyperlipoproteinemia Type I Hemoglobin A2 Genetic Variation Genes, Dominant DNA Mutational Analysis Genes, Lethal Crosses, Genetic Base Sequence Hemoglobins, Abnormal Hemochromatosis Polymerase Chain Reaction Ataxia Telangiectasia Genetic Predisposition to Disease Point Mutation Haplotypes Hyperlipoproteinemia Type II Mutation, Missense Molecular Sequence Data Cystinuria Hypobetalipoproteinemias Tay-Sachs Disease Exons Hemoglobin E Jews Adenine Phosphoribosyltransferase Genetic Linkage Mice, Mutant Strains Models, Genetic Fetal Hemoglobin alpha-Thalassemia Genetic Testing Polymorphism, Single Nucleotide Hemoglobinopathies Chromosome Mapping Inbreeding Genetics, Population Shrews Mice, Knockout Sandhoff Disease Polymorphism, Restriction Fragment Length beta-Thalassemia Glucosephosphate Dehydrogenase Deficiency DNA Genetic Markers Amino Acid Metabolism, Inborn Errors Phenylketonurias Microsatellite Repeats Globins Frameshift Mutation Selection, Genetic Lipid Metabolism, Inborn Errors Case-Control Studies Metabolism, Inborn Errors Codon, Nonsense Fabry Disease Hypolipoproteinemias Consanguinity Hybrid Vigor Hexosaminidase A Gene Deletion Homocystinuria Mice, Inbred C57BL Lipidoses Lecithin Acyltransferase Deficiency Cystic Fibrosis Apolipoproteins B Crossing Over, Genetic Electrophoresis, Starch Gel Lesch-Nyhan Syndrome DNA Primers Lipoprotein Lipase Ethylnitrosourea Apolipoprotein B-100 Genes Sequence Analysis, DNA Haploidy alpha 1-Antitrypsin Deficiency Albinism Chromosome Inversion Hemoglobin, Sickle Sequence Deletion beta-N-Acetylhexosaminidases Fibroblasts Hyperlipoproteinemias 2-Aminopurine Amino Acid Sequence Linkage Disequilibrium Asian Continental Ancestry Group

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