Male clinical homozygote. Medical search. Frequent questions

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Anatomy2

Chromosomes Embryo, Mammalian

Organisms7

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

Diseases26

Genetic Predisposition to Disease Hemochromatosis Albinism Hyperlipoproteinemia Type II Hyperlipoproteinemia Type III Ataxia Telangiectasia Gaucher Disease Xanthomatosis Thalassemia alpha 1-Antitrypsin Deficiency Polycythemia Hypolipoproteinemias alpha-Thalassemia Embryo Loss Gilbert Disease Cystic Fibrosis Hemoglobinopathies Polydactyly Familial Mediterranean Fever Metabolism, Inborn Errors Neural Tube Defects Lipid Metabolism, Inborn Errors Wolman Disease Siderosis Lecithin Acyltransferase Deficiency Fetal Death

Chemicals and Drugs48

Apolipoprotein E2 Catechol O-Methyltransferase Methylenetetrahydrofolate Reductase (NADPH2)Genetic Markers Histocompatibility Antigens Class I Ferritins Apolipoproteins E Hemoglobin E Membrane Proteins Ethylnitrosourea Oxidoreductases Acting on CH-NH Group Donors Hemoglobins, Abnormal DNA Apolipoproteins A DNA Primers Valine Serotonin Plasma Membrane Transport Proteins Transferrin Peptidyl-Dipeptidase A Apolipoprotein E4 Apolipoprotein C-III Codon Cholesterol Iron Aryl Hydrocarbon Hydroxylases Apolipoproteins B Homocysteine Apolipoprotein A-I Lipids Proline Lipoproteins Sitosterols Apolipoproteins C Triglycerides Fetal Hemoglobin Cholesterol, HDL Cholesterol Ester Transfer Proteins Deoxyribonucleases, Type II Site-Specific Apolipoprotein E3 Folic Acid Cystic Fibrosis Transmembrane Conductance Regulator Carrier Proteins MNSs Blood-Group System RNA, Messenger Factor V Globins Lipoproteins, LDL HLA Antigens

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Heterozygote Detection Case-Control Studies Pedigree Polymerase Chain Reaction Crosses, Genetic Genetic Association Studies Risk Factors Genetic Testing DNA Mutational Analysis Amino Acid Substitution Chromosome Mapping Models, Genetic Cohort Studies Odds Ratio Reference Values Risk Genotyping Techniques Inbreeding Electrophoresis, Starch Gel Gene Targeting Sequence Analysis, DNA Analysis of Variance

Phenomena and Processes39

Homozygote Heterozygote Genotype Polymorphism, Genetic Alleles Gene Frequency Genetic Predisposition to Disease Polymorphism, Single Nucleotide Mutation Phenotype Haplotypes Genetic Variation Genes, Lethal Genes, Recessive Polymorphism, Restriction Fragment Length Point Mutation Base Sequence Linkage Disequilibrium Genetic Markers Exons Mutation, Missense Genes, Dominant Amino Acid Substitution Genetic Linkage Hair Color Promoter Regions, Genetic Odds Ratio Eye Color Genes Codon Gene Deletion Risk Inbreeding Penetrance Selection, Genetic Chromosomes Amino Acid Sequence Introns Epistasis, Genetic

Disciplines and Occupations1

Genetics, Population

Information Science4

Base Sequence Molecular Sequence Data Publication Bias Amino Acid Sequence

Named Groups4

Asian Continental Ancestry Group European Continental Ancestry Group Jews Ethnic Groups

Health Care9

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

Geographicals2

Czech Republic China

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 Genotype Polymorphism, Genetic Alleles Gene Frequency Genetic Predisposition to Disease Polymorphism, Single Nucleotide Hemochromatosis Mutation Phenotype Haplotypes Heterozygote Detection Genetic Variation Case-Control Studies Genes, Lethal Mice, Mutant Strains Apolipoprotein E2 Genes, Recessive Catechol O-Methyltransferase Albinism Hyperlipoproteinemia Type II Pedigree Methylenetetrahydrofolate Reductase (NADPH2)Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Crosses, Genetic Genetic Association Studies Point Mutation Base Sequence Risk Factors Asian Continental Ancestry Group Genetic Testing Linkage Disequilibrium European Continental Ancestry Group Molecular Sequence Data Genetic Markers Exons Mutation, Missense Genes, Dominant DNA Mutational Analysis Hyperlipoproteinemia Type III Ataxia Telangiectasia Amino Acid Substitution Histocompatibility Antigens Class I Chromosome Mapping Genetic Linkage Ferritins Gaucher Disease Apolipoproteins E Models, Genetic Xanthomatosis Hemoglobin E Hair Color Membrane Proteins Ethylnitrosourea Thalassemia Oxidoreductases Acting on CH-NH Group Donors Jews alpha 1-Antitrypsin Deficiency Hemoglobins, Abnormal DNA Apolipoproteins A Promoter Regions, Genetic Genetics, Population Cohort Studies DNA Primers Valine Odds Ratio Serotonin Plasma Membrane Transport Proteins Reference Values Transferrin Eye Color Peptidyl-Dipeptidase A Apolipoprotein E4 Apolipoprotein C-III Genes Polycythemia Codon Hypolipoproteinemias alpha-Thalassemia Cholesterol Embryo Loss Iron Czech Republic Gene Deletion Drosophila melanogaster Mice, Neurologic Mutants Age of Onset Risk Gilbert Disease Aryl Hydrocarbon Hydroxylases Genotyping Techniques Cystic Fibrosis Apolipoproteins B Homocysteine Inbreeding China Penetrance Apolipoprotein A-I

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