Loss of HeterozygosityGene DeletionHeterozygoteChromosome DeletionSequence DeletionMicrosatellite RepeatsAllelesMutationBase SequenceChromosome MappingMolecular Sequence DataGenetic MarkersChromosomes, Human, Pair 17Genes, Tumor SuppressorChromosomes, Human, Pair 3DNA, NeoplasmPolymerase Chain ReactionChromosomes, Human, Pair 9HomozygoteChromosomes, Human, Pair 11Genetic VariationChromosomes, Human, Pair 1DNA Mutational AnalysisPolymorphism, GeneticHeterozygote DetectionGenotypeChromosomes, Human, Pair 10PedigreeChromosomes, Human, Pair 13PhenotypePolymorphism, Single-Stranded ConformationalInbreedingChromosomes, Human, Pair 16Chromosomes, Human, Pair 22ExonsPolymorphism, Restriction Fragment LengthGenetics, PopulationGene FrequencyAmino Acid SequenceDNA PrimersGenes, p53DNA, SatelliteGenes, DCCModels, GeneticChromosome AberrationsTumor Suppressor ProteinsIn Situ Hybridization, FluorescenceGene DosageRecombination, GeneticPoint MutationChromosomes, Human, Pair 6Sequence Analysis, DNAChromosomes, Human, Pair 5Genetic LociBlotting, SouthernPolymorphism, Single NucleotideGerm-Line MutationFrameshift MutationChromosomes, Human, Pair 7Chromosomes, Human, Pair 8Genetic LinkageDNAMice, KnockoutChromosomes, Human, Pair 19Promoter Regions, GeneticChromosomes, Human, Pair 18DNA-Binding ProteinsUniparental DisomyAcid Anhydride HydrolasesCrosses, GeneticHybrid VigorKaryotypingGenes, RetinoblastomaGenes, MCCChromosomes, Human, Pair 4HaplotypesWilms TumorAllelic ImbalanceGenes, Neurofibromatosis 1Cloning, MolecularRNA, MessengerGenetic Predisposition to DiseaseTranscription FactorsGenes, p16Mice, Inbred C57BLCyclin-Dependent Kinase Inhibitor p16PlasmidsEndangered SpeciesDNA MethylationAdenocarcinomaCell LineBreast NeoplasmsMutagenesisNeoplasm ProteinsTumor Suppressor Protein p53Repetitive Sequences, Nucleic AcidTranscription, GeneticMutation, MissenseNuclear ProteinsGenome, Human