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Gene DuplicationChromosome DuplicationChromosomesDNA ReplicationChromosome MappingChromosome BandingX ChromosomeChromosome AberrationsSex ChromosomesChromosomes, Human, Pair 1Chromosomes, HumanSegmental Duplications, GenomicChromosomes, BacterialChromosomes, Human, Pair 17Chromosomes, Human, Pair 7Chromosome SegregationChromosome DeletionChromosomes, Human, Pair 11Chromosomes, PlantChromosomes, Human, Pair 6Chromosomes, Human, Pair 9Evolution, MolecularChromosomes, Human, Pair 21Chromosomes, FungalChromosomes, Human, Pair 16Chromosomes, Human, Pair 22Chromosomes, Human, 6-12 and XChromosomes, Human, Pair 2Molecular Sequence DataChromosomes, Artificial, BacterialChromosomes, Human, XChromosome DisordersChromosomes, MammalianIn Situ Hybridization, FluorescenceChromosomes, Human, Pair 15Chromosomes, Human, Pair 10Chromosomes, Human, YKaryotypingChromosomes, Human, Pair 13Chromosomes, Human, Pair 4Chromosomes, Human, Pair 8Multigene FamilyChromosome PairingBase SequenceChromosomes, Human, Pair 19Chromosomes, Human, Pair 5Chromosomes, Human, Pair 12Chromosomes, Human, 1-3Chromosome BreakagePhylogenyChromosome PaintingChromosome InversionChromosomes, Human, Pair 14Genetic LinkageChromosomes, Human, Pair 18Chromosomes, Artificial, YeastChromosomes, Human, Pair 20Chromosomes, Human, 16-18Genes, DuplicateChromosomes, Human, 13-15Genetic MarkersChromosomes, Human, 21-22 and YRing ChromosomesRecombination, GeneticMutationAmino Acid SequenceTranslocation, GeneticCentromereChromosome PositioningModels, GeneticChromosomes, Human, 4-5X Chromosome InactivationSequence Analysis, DNAPhenotypeChromosomes, InsectMeiosisGene DosageMitosisAneuploidyPedigreeCloning, MolecularRepetitive Sequences, Nucleic AcidGenomeHybrid CellsAllelesChromosome StructuresSequence AlignmentTrisomyCrosses, GeneticGene RearrangementMetaphaseMicrosatellite RepeatsChromosomes, Human, 19-20Abnormalities, MultiplePolyploidyTandem Repeat SequencesDNASequence Homology, Nucleic AcidGenome, PlantBlotting, Southern

Integrative genomic analysis implicates gain of PIK3CA at 3q26 and MYC at 8q24 in chronic lymphocytic leukemia. (57/99)

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A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men. (58/99)

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Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot. (59/99)

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Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1q. (60/99)

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Electric oscillation and coupling of chromatin regulate chromosome packaging and transcription in eukaryotic cells. (61/99)

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NF-kappaB signalling requirement for brain myelin formation is shown by genotype/MRI phenotype correlations in patients with Xq28 duplications. (62/99)

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Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms. (63/99)

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16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. (64/99)

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