Susceptibility genes brca2. Medical search. Frequent questions

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Anatomy9

Chromosomes, Human, Pair 6 Tumor Cells, Cultured Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 10

Organisms2

Mice, Congenic Mice, Inbred C57BL

Diseases11

Breast Neoplasms Ovarian Neoplasms Genetic Predisposition to Disease Disease Susceptibility Neoplastic Syndromes, Hereditary Breast Neoplasms, Male Diabetes Mellitus, Type 1 Lupus Erythematosus, Systemic Retinoblastoma Psoriasis Disease Models, Animal

Chemicals and Drugs17

BRCA1 Protein BRCA2 Protein Neoplasm Proteins Transcription Factors Rad51 Recombinase Genetic Markers Anti-Bacterial Agents DNA-Binding Proteins Retinoblastoma Protein Carrier Proteins Endosomal Sorting Complexes Required for Transport Nuclear Proteins Tumor Suppressor Proteins Nod2 Signaling Adaptor Protein Protein Tyrosine Phosphatase, Non-Receptor Type 22 Neuregulin-1 HLA-DRB1 Chains

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Genetic Testing Chromosome Mapping Case-Control Studies Microbial Sensitivity Tests Genome-Wide Association Study Pedigree Genetic Association Studies DNA Mutational Analysis Polymerase Chain Reaction Models, Genetic Risk Factors Heterozygote Detection Sequence Analysis, DNA Disease Models, Animal Cohort Studies

Psychiatry and Psychology4

Schizophrenia Family Nuclear Family Autistic Disorder

Phenomena and Processes46

Genes, BRCA1 Genes, BRCA2 Genetic Predisposition to Disease Disease Susceptibility Germ-Line Mutation Heterozygote Mutation Genetic Linkage Polymorphism, Single Nucleotide Genotype DNA Repair Haplotypes Alleles DNA Damage Lod Score Linkage Disequilibrium Gene Frequency Genetic Markers Polymorphism, Genetic Phenotype Chromosomes, Human, Pair 6 Microsatellite Repeats Genome, Human Genetic Variation Genetic Loci Founder Effect Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 13 Genes, Retinoblastoma Genetic Heterogeneity Chromosomes, Human, Pair 2 Exons Chromosomes, Human, Pair 17 Penetrance Chromosomes, Human, Pair 5 Mutation, Missense Quantitative Trait Loci Epistasis, Genetic Chromosomes, Human, Pair 20 Base Sequence Chromosomes, Human, Pair 10 Drug Resistance, Bacterial Drug Resistance, Microbial Promoter Regions, Genetic Loss of Heterozygosity Multifactorial Inheritance

Disciplines and Occupations1

Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Nuclear Family

Information Science2

Molecular Sequence Data Base Sequence

Named Groups3

Jews Asian Continental Ancestry Group European Continental Ancestry Group

Health Care8

Genetic Testing Case-Control Studies Genome-Wide Association Study Family Health Risk Factors Age of Onset Genetic Counseling Cohort Studies

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

BRCA1 Protein Genes, BRCA1 BRCA2 Protein Genes, BRCA2 Breast Neoplasms Ovarian Neoplasms Genetic Predisposition to Disease Neoplasm Proteins Transcription Factors Disease Susceptibility Germ-Line Mutation Genetic Testing Heterozygote Mutation Genetic Linkage Polymorphism, Single Nucleotide Genotype Rad51 Recombinase Chromosome Mapping DNA Repair Haplotypes Alleles DNA Damage Lod Score Case-Control Studies Linkage Disequilibrium Gene Frequency Genetic Markers Microbial Sensitivity Tests Genome-Wide Association Study Pedigree Polymorphism, Genetic Phenotype Chromosomes, Human, Pair 6 Family Health Microsatellite Repeats Jews Neoplastic Syndromes, Hereditary Genome, Human Genetic Variation Genetic Association Studies Anti-Bacterial Agents DNA Mutational Analysis Tumor Cells, Cultured Genetic Loci Founder Effect Chromosomes, Human, Pair 1 Schizophrenia Chromosomes, Human, Pair 13 Genes, Retinoblastoma Polymerase Chain Reaction Molecular Sequence Data Models, Genetic Genetic Heterogeneity Chromosomes, Human, Pair 2 Risk Factors Age of Onset Asian Continental Ancestry Group DNA-Binding Proteins Family Nuclear Family Breast Neoplasms, Male Diabetes Mellitus, Type 1 Retinoblastoma Protein Carrier Proteins Exons Chromosomes, Human, Pair 17 Heterozygote Detection Penetrance Chromosomes, Human, Pair 5 European Continental Ancestry Group Mutation, Missense Endosomal Sorting Complexes Required for Transport Quantitative Trait Loci Epistasis, Genetic Lupus Erythematosus, Systemic Nuclear Proteins Chromosomes, Human, Pair 20 Base Sequence Chromosomes, Human, Pair 10 Genetic Counseling Drug Resistance, Bacterial Tumor Suppressor Proteins Nod2 Signaling Adaptor Protein Sequence Analysis, DNA Mice, Congenic Drug Resistance, Microbial Retinoblastoma Promoter Regions, Genetic Protein Tyrosine Phosphatase, Non-Receptor Type 22 Psoriasis Mice, Inbred C57BL Loss of Heterozygosity Multifactorial Inheritance Neuregulin-1 Autistic Disorder HLA-DRB1 Chains Disease Models, Animal Cohort Studies

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