CytogeneticsMolecular BiologyCytogenetic AnalysisChromosome AberrationsKaryotypingGeneticsMutationIn Situ Hybridization, FluorescenceLynch Syndrome IIPhenotypeGenetic TestingGenetics, PopulationChromosome MappingLeukemia, Myeloid, AcuteTranslocation, GeneticGenetic MarkersGenetic Predisposition to DiseaseMyelodysplastic SyndromesChromosome BandingChromosomes, HumanGenotypeLeukemia, MyeloidGenetic Diseases, InbornChromosome DisordersEye Diseases, HereditaryGenetic TechniquesPrognosisGenetic LinkageGenetic CounselingMolecular Sequence DataHeterotaxy SyndromeChromosome PaintingGenetic VariationPrenatal DiagnosisTwin Studies as TopicInterphaseAllelesNeoplastic Syndromes, HereditaryBase SequenceMonosomyPedigreeAbnormal KaryotypeTrisomyAneuploidyPolymerase Chain ReactionDNA Mutational AnalysisKaryotypeSyndromeGenetics, BehavioralRemission InductionGenome, HumanGenetic HeterogeneityModels, Geneticfms-Like Tyrosine Kinase 3Polymorphism, GeneticHeterozygote DetectionGenome-Wide Association StudyPolymorphism, Single NucleotidePseudoxanthoma ElasticumChromosomes, Human, Pair 11GenomicsLeukemia, Myelomonocytic, AcuteChromosome DeletionMicrosatellite RepeatsChromosomes, Human, Pair 8Evolution, MolecularSequence Analysis, DNAAcute DiseaseHair ColorHistory, 20th CenturyAbnormalities, MultipleGene Expression ProfilingMetaphaseAmino Acid SequenceNeoplasms, Adipose TissueChromosomes, Human, Pair 13Chromosome InversionQuantitative Trait LociXanthomatosisGene DeletionDisease Models, AnimalIndividualized MedicineChromosomes, Human, Pair 15Genes, DominantChromosomes, Human, Pair 5Chromosomes, Human, Pair 14Models, BiologicalGene RearrangementChromosomes, Human, Pair 18Biological EvolutionDNA, PlantChromosomes, Human, Pair 7LaboratoriesPhylogenyX ChromosomePolymorphism, Restriction Fragment LengthCrosses, GeneticCytarabineBlotting, SouthernDNA