Loss of HeterozygosityHomozygoteChromosomes, Human, Pair 9Survival of Motor Neuron 2 ProteinSurvival of Motor Neuron 1 ProteinSMN Complex ProteinsMuscular Atrophy, SpinalGene DeletionHeterozygoteMicrosatellite RepeatsAllelesGenes, Tumor SuppressorGenetic MarkersChromosomes, Human, Pair 17Chromosome DeletionChromosomes, Human, Pair 3DNA, NeoplasmChromosome MappingChromosomes, Human, Pair 11MutationGenetic VariationChromosomes, Human, Pair 1Polymerase Chain ReactionPolymorphism, GeneticHeterozygote DetectionInbreedingChromosomes, Human, Pair 10Genetics, PopulationPolymorphism, Single-Stranded ConformationalGenotypeChromosomes, Human, Pair 13Chromosomes, Human, Pair 16DNA Mutational AnalysisPolymorphism, Restriction Fragment LengthGenes, DCCDNA, SatelliteGene FrequencyPedigreeGenes, p53Base SequenceTumor Suppressor ProteinsMolecular Sequence DataChromosomes, Human, Pair 6Chromosomes, Human, Pair 18Genetic LociGerm-Line MutationModels, GeneticChromosomes, Human, Pair 22Chromosomes, Human, Pair 5Polymorphism, Single NucleotideHybrid VigorGenes, MCCChromosome AberrationsChromosomes, Human, Pair 19ExonsChromosomes, Human, Pair 8PhenotypeAcid Anhydride HydrolasesUniparental DisomyGene DosageGenetic LinkageDNA PrimersChromosomes, Human, Pair 7Genes, RetinoblastomaAllelic ImbalanceEndangered SpeciesWilms TumorPoint MutationSequence DeletionGenes, Neurofibromatosis 1Sequence Analysis, DNACrosses, GeneticAdenocarcinomaBreast NeoplasmsRecombination, GeneticIn Situ Hybridization, FluorescenceChromosomes, Human, Pair 4DNA MethylationGenes, APCCarcinoma, Squamous CellHaplotypesGenes, p16Genetic Predisposition to DiseaseChromosomes, HumanChromosomal InstabilityDiploidySelection, GeneticNeoplasm ProteinsTumor Suppressor Protein p53BreedingBlotting, SouthernMicrodissectionElectrophoresis, Starch GelOvarian NeoplasmsMicrosatellite InstabilityKidney NeoplasmsFrameshift MutationCyclin-Dependent Kinase Inhibitor p16OligodendrogliomaGene Expression Regulation, Neoplastic