Loss of HeterozygosityAllelesHomozygoteChromosomes, Human, Pair 9Survival of Motor Neuron 2 ProteinSurvival of Motor Neuron 1 ProteinSMN Complex ProteinsMuscular Atrophy, SpinalGene DeletionHeterozygoteMicrosatellite RepeatsPolymorphism, GeneticGenotypeGenetic MarkersMutationGene FrequencyChromosome MappingGenetic VariationChromosome DeletionPolymerase Chain ReactionGenes, Tumor SuppressorChromosomes, Human, Pair 17Chromosomes, Human, Pair 3DNA, NeoplasmPolymorphism, Single NucleotideChromosomes, Human, Pair 11Base SequenceHeterozygote DetectionGenetics, PopulationMolecular Sequence DataChromosomes, Human, Pair 1Polymorphism, Restriction Fragment LengthPhenotypeDNA Mutational AnalysisInbreedingGenetic Predisposition to DiseasePedigreeChromosomes, Human, Pair 10Polymorphism, Single-Stranded ConformationalHaplotypesModels, GeneticChromosomes, Human, Pair 16Chromosomes, Human, Pair 13DNA, SatelliteGenes, p53Genetic LociCrosses, GeneticExonsGenetic LinkageGenes, DCCSequence Analysis, DNADNA PrimersLinkage DisequilibriumTumor Suppressor ProteinsChromosomes, Human, Pair 6Point MutationGerm-Line MutationGene DosageSelection, GeneticRecombination, GeneticChromosomes, Human, Pair 5Chromosomes, Human, Pair 18Chromosomes, Human, Pair 22Sequence DeletionHybrid VigorChromosomes, Human, Pair 8Chromosomes, Human, Pair 19Chromosome AberrationsAllelic ImbalanceCase-Control StudiesGenes, MCCDNAMutation, MissenseUniparental DisomyChromosomes, Human, Pair 7Acid Anhydride HydrolasesGenes, RetinoblastomaGenes, RecessiveEndangered SpeciesBlotting, SouthernWilms TumorDiploidyAmino Acid SequenceDNA MethylationGenes, DominantBreast NeoplasmsFrameshift MutationBreedingGenes, Neurofibromatosis 1AdenocarcinomaGenetic TestingChromosomes, Human, Pair 4Genome, HumanElectrophoresis, Starch GelIn Situ Hybridization, FluorescenceGenes, APCDNA, PlantAsian Continental Ancestry GroupTumor Suppressor Protein p53Carcinoma, Squamous Cell