Brca1 or brca2 mutation carriers. Medical search. Frequent questions

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Anatomy6

Fallopian Tubes Cell Line Cell Line, Tumor Chromosomes, Human, Pair 17 HeLa Cells Chromosomes, Human, Pair 6

Organisms2

Escherichia coli Saccharomyces cerevisiae

Diseases29

Breast Neoplasms Genetic Predisposition to Disease Ovarian Neoplasms Fallopian Tube Neoplasms Neoplastic Syndromes, Hereditary Colorectal Neoplasms, Hereditary Nonpolyposis Breast Neoplasms, Male Hereditary Breast and Ovarian Cancer Syndrome Romano-Ward Syndrome Cardiomyopathy, Hypertrophic, Familial Li-Fraumeni Syndrome Cystadenocarcinoma, Serous Paraganglioma Syndrome Dystonia Cardiomyopathy, Hypertrophic Neoplasms Genomic Instability Long QT Syndrome Colorectal Neoplasms Endometrial Neoplasms Microsatellite Instability Carcinoma Neoplasms, Second Primary Carcinoma, Ductal, Breast Parkinson Disease Peritoneal Neoplasms Dystonic Disorders Optic Atrophy, Hereditary, Leber

Chemicals and Drugs42

BRCA1 Protein BRCA2 Protein Carrier Proteins Neoplasm Proteins Rad51 Recombinase MutS Homolog 2 Protein DNA-Binding Proteins Transcription Factors Nuclear Proteins Codon, Nonsense Drug Carriers DNA, Neoplasm Tumor Suppressor Proteins Tumor Suppressor Protein p53 DNA Primers Ubiquitin-Protein Ligases Acyl Carrier Protein Phthalazines Adaptor Proteins, Signal Transducing DNA Glucosylceramidase Genetic Markers Protein-Serine-Threonine Kinases Presenilin-1 RNA, Messenger DNA Repair Enzymes Membrane Proteins Reduced Folate Carrier Protein Codon Plakophilins NAV1.5 Voltage-Gated Sodium Channel Receptors, Estrogen Ataxia Telangiectasia Mutated Proteins Proto-Oncogene Proteins Receptors, Progesterone Apoptosis Regulatory Proteins Mutant Proteins Bacterial Proteins Contraceptives, Oral Cell Cycle Proteins Tumor Markers, Biological Recombinant Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment38

Heterozygote Detection Genetic Testing Pedigree DNA Mutational Analysis Salpingectomy Polymerase Chain Reaction Case-Control Studies Ovariectomy Risk Factors Amino Acid Substitution Mastectomy Drug Carriers Sequence Analysis, DNA Risk Risk Assessment Genetic Association Studies Cohort Studies Mutagenesis, Site-Directed Models, Genetic Chromosome Mapping Immunohistochemistry Models, Molecular Transfection Prognosis Incidence Mammography Cloning, Molecular Salpingostomy Sequence Alignment Genetic Complementation Test Magnetic Resonance Imaging Retrospective Studies Reverse Transcriptase Polymerase Chain Reaction Registries Sterilization, Tubal Therapeutic Irrigation Odds Ratio Mutagenesis, Insertional

Psychiatry and Psychology1

Phenomena and Processes74

Genes, BRCA1 Genes, BRCA2 Heterozygote Germ-Line Mutation Mutation Mutation, Missense Point Mutation Genetic Predisposition to Disease Founder Effect Penetrance Frameshift Mutation Genotype Exons Phenotype Alleles DNA Mismatch Repair Polymorphism, Single-Stranded Conformational Base Sequence Amino Acid Substitution Mutation Rate Polymorphism, Single Nucleotide DNA Repair Homozygote Sequence Deletion Gene Frequency Polymorphism, Genetic Amino Acid Sequence Codon, Nonsense Genes, p53 Gene Deletion Risk Genes, Dominant Protein Structure, Tertiary Loss of Heterozygosity DNA Damage Mutagenesis Promoter Regions, Genetic Genetic Linkage Genetic Variation Gene Expression Regulation, Neoplastic Protein Binding Microsatellite Repeats Genes, Recessive Binding Sites Genetic Markers Sequence Homology, Amino Acid Haplotypes Transfection Chromosomes, Human, Pair 17 Recombination, Genetic Codon Genes, Tumor Suppressor Genomic Instability Transcription, Genetic Haploinsufficiency Base Pair Mismatch Suppression, Genetic Plasmids Genetic Heterogeneity Time Factors Homologous Recombination Microsatellite Instability DNA Methylation Gene Expression Kinetics Genes, Lethal Odds Ratio Chromosomes, Human, Pair 6 Genes, p16 Consanguinity Mutagenesis, Insertional Signal Transduction Introns Epistasis, Genetic

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science5

Base Sequence Molecular Sequence Data Amino Acid Sequence Incidence Registries

Named Groups2

Jews Asian Continental Ancestry Group

Health Care15

Genetic Testing Genetic Counseling Family Health Carrier State Age of Onset Case-Control Studies Risk Factors Risk Risk Assessment Cohort Studies Age Factors Incidence Retrospective Studies Registries Odds Ratio

Geographicals6

Iceland Israel Australia Canada District of Columbia North America

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 Geographicals

Genes, BRCA1 BRCA1 Protein BRCA2 Protein Genes, BRCA2 Heterozygote Germ-Line Mutation Mutation Mutation, Missense Point Mutation Breast Neoplasms Heterozygote Detection Genetic Testing Genetic Predisposition to Disease Ovarian Neoplasms Jews Pedigree Founder Effect DNA Mutational Analysis Penetrance Salpingectomy Frameshift Mutation Genotype Genetic Counseling Family Health Fallopian Tube Neoplasms Neoplastic Syndromes, Hereditary Carrier State Exons Phenotype Colorectal Neoplasms, Hereditary Nonpolyposis Alleles Carrier Proteins Breast Neoplasms, Male Polymerase Chain Reaction Age of Onset DNA Mismatch Repair Neoplasm Proteins Case-Control Studies Polymorphism, Single-Stranded Conformational Hereditary Breast and Ovarian Cancer Syndrome Base Sequence Rad51 Recombinase Molecular Sequence Data MutS Homolog 2 Protein Ovariectomy DNA-Binding Proteins Transcription Factors Risk Factors Amino Acid Substitution Mutation Rate Nuclear Proteins Polymorphism, Single Nucleotide DNA Repair Homozygote Sequence Deletion Gene Frequency Polymorphism, Genetic Amino Acid Sequence Codon, Nonsense Mastectomy Drug Carriers DNA, Neoplasm Tumor Suppressor Proteins Genes, p53 Gene Deletion Family Sequence Analysis, DNA Risk Romano-Ward Syndrome Risk Assessment Genetic Association Studies Cohort Studies Cardiomyopathy, Hypertrophic, Familial Genes, Dominant Mutagenesis, Site-Directed Protein Structure, Tertiary Tumor Suppressor Protein p53 Loss of Heterozygosity DNA Primers Fallopian Tubes Ubiquitin-Protein Ligases DNA Damage Mutagenesis Acyl Carrier Protein Promoter Regions, Genetic Genetic Linkage Genetic Variation Cell Line Phthalazines Adaptor Proteins, Signal Transducing Gene Expression Regulation, Neoplastic Protein Binding DNA Microsatellite Repeats Genes, Recessive Li-Fraumeni Syndrome Glucosylceramidase Models, Genetic Age Factors Cystadenocarcinoma, Serous

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