AnatomyOrganismsDiseasesChemicals and DrugsAnalytical, Diagnostic and Therapeutic Techniques and EquipmentPsychiatry and PsychologyPhenomena and ProcessesDisciplines and OccupationsAnthropology, Education, Sociology and Social PhenomenaTechnology, Industry, AgricultureInformation ScienceNamed GroupsHealth Care
Loss of HeterozygosityHomozygoteChromosomes, Human, Pair 9Survival of Motor Neuron 2 ProteinGenes, RecessiveSurvival of Motor Neuron 1 ProteinSMN Complex ProteinsMuscular Atrophy, SpinalGene DeletionHeterozygoteMicrosatellite RepeatsAllelesMutationPedigreeChromosome MappingGenetic MarkersConsanguinityChromosomes, Human, Pair 17Chromosome DeletionChromosomes, Human, Pair 3Genes, Tumor SuppressorDNA Mutational AnalysisDNA, NeoplasmHeterozygote DetectionChromosomes, Human, Pair 1Polymerase Chain ReactionChromosomes, Human, Pair 11Polymorphism, GeneticGenotypePhenotypeGenetic VariationGenetic LinkageBase SequenceInbreedingMolecular Sequence DataPolymorphism, Single-Stranded ConformationalChromosomes, Human, Pair 10Gene FrequencyChromosomes, Human, Pair 16Genetics, PopulationChromosomes, Human, Pair 13Polymorphism, Restriction Fragment LengthExonsGenes, DominantMutation, MissenseCrosses, GeneticModels, GeneticDNA, SatellitePolymorphism, Single NucleotideGenes, p53HaplotypesGenes, DCCChromosomes, Human, Pair 6SyndromePoint MutationPolycystic Kidney, Autosomal RecessiveFrameshift MutationGenetic LociChromosomes, Human, Pair 5Tumor Suppressor ProteinsChromosomes, Human, Pair 19Genetic Predisposition to DiseaseChromosomes, Human, Pair 18Chromosome AberrationsDNA PrimersSequence Analysis, DNACodon, NonsenseSequence DeletionChromosomes, Human, Pair 8Chromosomes, Human, Pair 22Germ-Line MutationChromosomes, Human, Pair 7Lod ScoreUniparental DisomyHybrid VigorGenes, LethalGene DosageGenes, MCCGenetic TestingRecombination, GeneticAmino Acid SequenceDiploidyAcid Anhydride HydrolasesRetinitis PigmentosaAbnormalities, MultipleChromosomes, Human, Pair 4X ChromosomeGenes, RetinoblastomaAllelic ImbalanceDNAEndangered SpeciesWilms TumorFounder EffectGenetic HeterogeneitySelection, GeneticBlotting, SouthernIn Situ Hybridization, FluorescenceIchthyosisChromosomes, Human, Pair 2Genes, Neurofibromatosis 1