Chromosome AberrationsIn Situ Hybridization, FluorescenceTranslocation, GeneticMutationKaryotypingLoss of HeterozygosityAbnormal KaryotypeChromosome DisordersOmanChromosomes, Human, Pair 17Sex Chromosome AberrationsTrisomyChromosome DeletionCytogenetic AnalysisCongenital AbnormalitiesChromosomes, Human, Pair 3Chromosomes, Human, Pair 11Genes, p53Chromosomes, Human, Pair 13Chromosomes, Human, Pair 14Comparative Genomic HybridizationChromosomes, Human, Pair 9Oncogene Proteins, FusionGlucosephosphate Dehydrogenase DeficiencyPhenotypeChromosomes, Human, Pair 1PedigreeChromosomes, Human, Pair 18Chromosomes, HumanPrognosisDNA Mutational AnalysisGene DeletionGene RearrangementGenetic TestingMultiple MyelomaChromosomes, Human, Pair 8AneuploidyDNA, NeoplasmPloidiesLeukemia, Myeloid, AcuteAbnormalities, MultiplePrecursor Cell Lymphoblastic Leukemia-LymphomaInfertility, MalePolymerase Chain ReactionLymphoma, Large B-Cell, DiffuseChromosomes, Human, Pair 7OligospermiaMyelodysplastic SyndromesPregnancyLeukemia, Lymphocytic, Chronic, B-CellCore Binding Factor Alpha 2 SubunitHeterozygoteGenes, Tumor SuppressorGene AmplificationPolymorphism, Single-Stranded ConformationalTumor Suppressor Protein p53Neoplasm ProteinsGenetic Predisposition to DiseaseDisease ProgressionHomozygoteNucleic Acid HybridizationGene Expression ProfilingImmunohistochemistryMicrosatellite RepeatsOligonucleotide Array Sequence AnalysisPrecancerous ConditionsImmunophenotypingCell Transformation, NeoplasticTumor Markers, BiologicalInfant, NewbornCyclin-Dependent Kinase Inhibitor p16Gene DosageChromosome MappingLung NeoplasmsGene Expression Regulation, NeoplasticBase SequenceGenes, rasReverse Transcriptase Polymerase Chain ReactionOncogenesDisease Models, AnimalProto-Oncogene ProteinsDNA-Binding ProteinsNeoplasmsGenetic MarkersAntineoplastic AgentsExonsRisk FactorsBrain NeoplasmsPoint MutationEye AbnormalitiesNuclear ProteinsGenotypeNeoplasm StagingMolecular Sequence DataCase-Control StudiesBlotting, SouthernAllelesRNA, MessengerTreatment OutcomeRecurrence