Brca2 founder mutation. Medical search. Frequent questions

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Anatomy2

Cell Line Cell Line, Tumor

Organisms4

Escherichia coli Mice, Transgenic Saccharomyces cerevisiae Drosophila

Diseases10

Genetic Predisposition to Disease Ovarian Neoplasms Breast Neoplasms Nijmegen Breakage Syndrome Neoplastic Syndromes, Hereditary Breast Neoplasms, Male Dystonia Musculorum Deformans Colorectal Neoplasms, Hereditary Nonpolyposis Syndrome Prostatic Neoplasms

Chemicals and Drugs25

BRCA1 Protein BRCA2 Protein Codon, Nonsense Neoplasm Proteins Transcription Factors Nuclear Proteins DNA-Binding Proteins Genetic Markers MutS Homolog 2 Protein Carrier Proteins DNA Primers Proteins DNA, Mitochondrial DNA DNA, Neoplasm Rad51 Recombinase Codon Membrane Proteins RNA, Messenger Tumor Suppressor Proteins Mutant Proteins Tumor Suppressor Protein p53 Drosophila Proteins RNA Splice Sites Bacterial Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Pedigree DNA Mutational Analysis Genetic Testing Heterozygote Detection Polymerase Chain Reaction Amino Acid Substitution Sequence Analysis, DNA Chromosome Mapping Case-Control Studies Mutagenesis, Site-Directed Models, Genetic Cohort Studies Models, Molecular Risk Factors Sequence Alignment Prevalence Cloning, Molecular Genetic Complementation Test Incidence Transfection Crosses, Genetic Mutagenesis, Insertional

Psychiatry and Psychology1

Phenomena and Processes62

Founder Effect Genes, BRCA1 Genes, BRCA2 Mutation Mutation, Missense Germ-Line Mutation Point Mutation Haplotypes Heterozygote Frameshift Mutation Exons Genetic Predisposition to Disease Genes, Recessive Homozygote Codon, Nonsense Genotype Alleles Gene Frequency Base Sequence Sequence Deletion Phenotype Penetrance Microsatellite Repeats Consanguinity Polymorphism, Single-Stranded Conformational Amino Acid Substitution Gene Deletion Genetic Linkage Mutation Rate Polymorphism, Single Nucleotide Amino Acid Sequence Linkage Disequilibrium Genetic Markers Genetic Variation Mutagenesis Protein Structure, Tertiary Genes, Dominant Polymorphism, Genetic DNA Repair Sequence Homology, Amino Acid Genes, p53 Protein Binding Promoter Regions, Genetic Binding Sites Codon Recombination, Genetic Suppression, Genetic Evolution, Molecular Transcription, Genetic Transfection Phylogeny Exome Plasmids Genes, Lethal Introns Mutagenesis, Insertional Genetic Heterogeneity Polymorphism, Restriction Fragment Length Loss of Heterozygosity Signal Transduction RNA Splice Sites Selection, Genetic

Disciplines and Occupations2

Genetics, Population Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Humanities1

History, 17th Century

Information Science6

Base Sequence Molecular Sequence Data Amino Acid Sequence Prevalence Incidence Phylogeny

Named Groups4

Jews Gypsies Arabs Infant, Newborn

Health Care9

Genetic Testing Family Health Age of Onset Case-Control Studies Cohort Studies Risk Factors Genetic Counseling Prevalence Incidence

Geographicals7

Africa, Northern Israel Finland Tunisia Middle East France Italy

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 Humanities Information Science Named Groups Health Care Geographicals

Founder Effect Genes, BRCA1 BRCA1 Protein BRCA2 Protein Genes, BRCA2 Jews Mutation Mutation, Missense Pedigree Germ-Line Mutation Point Mutation DNA Mutational Analysis Genetic Testing Haplotypes Heterozygote Frameshift Mutation Gypsies Africa, Northern Exons Genetic Predisposition to Disease Ovarian Neoplasms Genes, Recessive Breast Neoplasms Homozygote Codon, Nonsense Genotype Alleles Gene Frequency Base Sequence Family Health Nijmegen Breakage Syndrome Sequence Deletion Phenotype Neoplastic Syndromes, Hereditary Heterozygote Detection Molecular Sequence Data Penetrance Microsatellite Repeats Israel Age of Onset Consanguinity Polymorphism, Single-Stranded Conformational History, 17th Century Polymerase Chain Reaction Finland Amino Acid Substitution Tunisia Breast Neoplasms, Male Middle East Gene Deletion Arabs Sequence Analysis, DNA Genetic Linkage Chromosome Mapping Mutation Rate Dystonia Musculorum Deformans Genetics, Population Neoplasm Proteins Polymorphism, Single Nucleotide Amino Acid Sequence Colorectal Neoplasms, Hereditary Nonpolyposis Transcription Factors Linkage Disequilibrium Nuclear Proteins DNA-Binding Proteins Syndrome Family Genetic Markers MutS Homolog 2 Protein France Genetic Variation Italy Carrier Proteins Case-Control Studies Mutagenesis, Site-Directed Mutagenesis Models, Genetic DNA Primers Protein Structure, Tertiary Genes, Dominant Proteins Polymorphism, Genetic Cell Line DNA, Mitochondrial DNA Repair Cohort Studies Sequence Homology, Amino Acid Genes, p53 Models, Molecular Risk Factors Protein Binding DNA DNA, Neoplasm Promoter Regions, Genetic Rad51 Recombinase Binding Sites Codon Genetic Counseling Recombination, Genetic Escherichia coli

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