Loss of HeterozygosityHeterozygoteGenetic MarkersMicrosatellite RepeatsBiological MarkersAllelesChromosome MappingChromosomes, Human, Pair 17Genes, Tumor SuppressorChromosome DeletionChromosomes, Human, Pair 3DNA, NeoplasmChromosomes, Human, Pair 9Polymerase Chain ReactionGenetic VariationMutationPolymorphism, GeneticTumor Markers, BiologicalChromosomes, Human, Pair 11Chromosomes, Human, Pair 1GenotypeHomozygoteGene DeletionHeterozygote DetectionInbreedingGenetics, PopulationChromosomes, Human, Pair 10PedigreePolymorphism, Restriction Fragment LengthBase SequenceChromosomes, Human, Pair 16Gene FrequencyChromosomes, Human, Pair 13DNA Mutational AnalysisPolymorphism, Single-Stranded ConformationalGenetic LinkageDNA, SatelliteMolecular Sequence DataGenes, DCCPhenotypeGenes, p53Polymorphism, Single NucleotideModels, GeneticGenetic LociTumor Suppressor ProteinsChromosomes, Human, Pair 6DNA PrimersChromosomes, Human, Pair 18ImmunohistochemistryChromosomes, Human, Pair 5Chromosomes, Human, Pair 22Chromosome AberrationsSequence Analysis, DNAChromosomes, Human, Pair 19Germ-Line MutationCrosses, GeneticHybrid VigorChromosomes, Human, Pair 8ExonsHaplotypesGene DosageChromosomes, Human, Pair 7Breast NeoplasmsGenes, MCCRecombination, GeneticEndangered SpeciesAcid Anhydride HydrolasesUniparental DisomyAdenocarcinomaAllelic ImbalancePoint MutationGenetic Predisposition to DiseaseNeoplasm ProteinsGenes, RetinoblastomaIn Situ Hybridization, FluorescenceWilms TumorDNA, PlantSequence DeletionCarcinoma, Squamous CellBreedingDNA MethylationChromosomes, Human, Pair 4PrognosisGenes, Neurofibromatosis 1Linkage DisequilibriumChromosomes, HumanSelection, GeneticTumor Suppressor Protein p53Ovarian NeoplasmsBlotting, SouthernDiploidyDNAReverse Transcriptase Polymerase Chain ReactionGenes, APCGenome, HumanKaryotypingColorectal NeoplasmsGenes, p16MicrodissectionDisease Progression