Chromosomal duplication

Chromosome, Chromosome abnormality, Chromosomal translocation, Chromosomal inversion, Y-chromosomal Adam, Chromosome instability, Y chromosome, Chromosomal rearrangement, Chromosome 13, Chromosomal deletion syndrome, Chromosome instability syndrome, Polytene chromosome, Chromosome 15, Chromosome 2, Satellite chromosome, Y-chromosomal Aaron, Balancer chromosome, Circular chromosome, Chromosome 21, Chromosome 5, Chromosome 22, X chromosome, Homologous chromosome, Chromosome segregation, Chromosome 7, Holocentric chromosome, Chromosomal fragile site, Chromosome regions, B chromosome, Sex chromosome, Chromosomal polymorphism, Ring chromosome 20 syndrome, Small supernumerary marker chromosome, Ring chromosome 22, Chromosome 17, Human Y-chromosome DNA haplogroup, Chromosome 15q partial deletion, Chromosome 6, Chromosome 4, Y Chromosome Consortium, Chromosome 9

Chromosome 18, Chromosome condensation, Chromosome 3, Chromosome 12, Chromosome 14, Chromosome 11, Chromosome 1, Yeast artificial chromosome, Chromosome engineering, Chromosome 20, Philadelphia chromosome, Eukaryotic chromosome structure, Chromosome 16, Chromosome 8, Chromosome 10, Chromosome 19, Ring chromosome 14 syndrome, Sex chromosome anomalies, Chromosome conformation capture, Normalized chromosome value, List of organisms by chromosome count, Ring chromosome 15, Segmental duplication on the human Y chromosome, Artificial chromosome, Y chromosome microdeletion, Chromosomal crossover, Boveri–Sutton chromosome theory, Chromosome territories, Nondisjunction, Ring chromosome, Karyotype, Y Chromosome Haplotype Reference Database, Ring chromosome 18, Dicentric chromosome, Sex-chromosome dosage compensation, Chromosome (evolutionary algorithm), Aneuploidy, Trisomy 16, Conversion table for Y chromosome haplogroups, Cytogenetics, Chromosome 15q trisomy, Human artificial chromosome, The Calcutta Chromosome, Bacterial artificial chromosome, Trisomy 8, Thymosin beta-4, Y-chromosomal, Trisomy 9, Chromosome 2q deletion, Trisomy, Chromosome jumping

Chromosome, Chromosome abnormality, Chromosomal translocation, Chromosomal inversion, Y-chromosomal Adam, Chromosome instability, Y chromosome, Chromosomal rearrangement, Chromosome 13, Chromosomal deletion syndrome, Chromosome instability syndrome, Polytene chromosome, Chromosome 15, Chromosome 2, Satellite chromosome, Y-chromosomal Aaron, Balancer chromosome, Circular chromosome, Chromosome 21, Chromosome 5, Chromosome 22, X chromosome, Homologous chromosome, Chromosome segregation, Chromosome 7, Holocentric chromosome, Chromosomal fragile site, Chromosome regions, B chromosome, Sex chromosome, Chromosomal polymorphism, Ring chromosome 20 syndrome, Small supernumerary marker chromosome, Ring chromosome 22, Chromosome 17, Human Y-chromosome DNA haplogroup, Chromosome 15q partial deletion, Chromosome 6, Chromosome 4, Y Chromosome Consortium, Chromosome 9, Chromosome 18, Chromosome condensation, Chromosome 3, Chromosome 12, Chromosome 14, Chromosome 11, Chromosome 1, Yeast artificial chromosome, Chromosome engineering, Chromosome 20, Philadelphia chromosome, Eukaryotic chromosome structure, Chromosome 16, Chromosome 8, Chromosome 10, Chromosome 19, Ring chromosome 14 syndrome, Sex chromosome anomalies, Chromosome conformation capture, Normalized chromosome value, List of organisms by chromosome count, Ring chromosome 15, Segmental duplication on the human Y chromosome, Artificial chromosome, Y chromosome microdeletion, Chromosomal crossover, Boveri–Sutton chromosome theory, Chromosome territories, Nondisjunction, Ring chromosome, Karyotype, Y Chromosome Haplotype Reference Database, Ring chromosome 18, Dicentric chromosome, Sex-chromosome dosage compensation, Chromosome (evolutionary algorithm), Aneuploidy, Trisomy 16, Conversion table for Y chromosome haplogroups, Cytogenetics, Chromosome 15q trisomy, Human artificial chromosome, The Calcutta Chromosome, Bacterial artificial chromosome, Trisomy 8, Thymosin beta-4, Y-chromosomal, Trisomy 9, Chromosome 2q deletion, Trisomy, Chromosome jumping, Chromosome No. 1 syndrome, Polycentric chromosome, Distal trisomy 10q, Chromosome 1 open reading frame 194, ZW sex-determination system, Genes, Chromosomes & Cancer, Isochromosome, XY sex-determination system, Gene duplication, Micronucleus, 3p deletion syndrome, Chromosome 12 open reading frame 71, Deletion (genetics), Primer walking, Autosome, Centromere, X-inactivation, Monosomy 9p, Tetrasomy 9p, Trisomy 22, Chromosome landing, Chromosome microdissection, Chromosome 2q31.1 duplication syndrome gene, Monocentric chromosome, Isodicentric 15, DECIPHER, Double minute, Microcell-mediated chromosome transfer, Mosaic (genetics), Chromosome X open reading frame 57, Trisomy 18, Eukaryotic chromosome fine structure, XYY syndrome, Derivative chromosome, Locus (genetics), Marker chromosome, Non-random segregation of chromosomes, Comparative genomic hybridization, Microchromosome, Lampbrush chromosome, Chromosome 5q deletion syndrome, Chromosome scaffold, Control of chromosome duplication, Ploidy, Bivalent (genetics), Fluorescence in situ hybridization, List of Y-chromosome haplogroups in populations of the world, Wolf–Hirschhorn syndrome, Dup15q, Secondary chromosome, Linear chromosome, 1p36 deletion syndrome, Cell division, Premature chromosome condensation, C5orf52, Jacobsen syndrome, Parasitic chromosome, Microfluidic whole genome haplotyping, Mosaic loss of chromosome Y, Supernumerary chromosome