Chromosome duplication

Chromosome, Chromosome abnormality, Y chromosome, Chromosome 2, Chromosome 13, X chromosome, Chromosome 21, Chromosome 17, Chromosome 5, Chromosome 15, Chromosome 4, Chromosome 7, Chromosome 9, Chromosome 18, Chromosome 22, Chromosome 3, Circular chromosome, Chromosome 1, Chromosome 14, Chromosome 12, Chromosome 6, Balancer chromosome, Sex chromosome, Chromosome instability, Chromosome 11, Y chromosome microdeletion, Chromosome 20, Chromosome regions, Chromosome 8, Chromosome 16, B chromosome, Chromosome 10, Chromosome 19, Chromosome condensation, Satellite chromosome, Polytene chromosome, Yeast artificial chromosome, Artificial chromosome, Ring chromosome 15, Chromosomal inversion, Small supernumerary marker chromosome

Ring chromosome 20 syndrome, Ring chromosome 14 syndrome, Chromosome territories, Chromosomal translocation, Boveri–Sutton chromosome theory, Ring chromosome 18, Homologous chromosome, Philadelphia chromosome, Ring chromosome 22, Chromosome (evolutionary algorithm), Eukaryotic chromosome structure, Chromosome 15q trisomy, Chromosome segregation, Ring chromosome, Human Y-chromosome DNA haplogroup, Y-chromosomal Adam, Sex chromosome anomalies, Y Chromosome Consortium, The Calcutta Chromosome, Human artificial chromosome, Chromosome 2q deletion, Sex-chromosome dosage compensation, Chromosome instability syndrome, Chromosome 15q partial deletion, Holocentric chromosome, Chromosomal rearrangement, Bacterial artificial chromosome, Chromosome conformation capture, Chromosome 1 open reading frame 194, Chromosomal deletion syndrome, Segmental duplication on the human Y chromosome, Chromosome engineering, Normalized chromosome value, Chromosomal fragile site, Monocentric chromosome, Derivative chromosome, Chromosome 2q31.1 duplication syndrome gene, Microcell-mediated chromosome transfer, List of organisms by chromosome count, Conversion table for Y chromosome haplogroups, Y-chromosomal Aaron, Chromosome X open reading frame 57, Chromosome jumping, Y Chromosome Haplotype Reference Database, Chromosome scaffold, Lampbrush chromosome, Karyotype, Dicentric chromosome, Marker chromosome, Trisomy 8

Chromosome, Chromosome abnormality, Y chromosome, Chromosome 2, Chromosome 13, X chromosome, Chromosome 21, Chromosome 17, Chromosome 5, Chromosome 15, Chromosome 4, Chromosome 7, Chromosome 9, Chromosome 18, Chromosome 22, Chromosome 3, Circular chromosome, Chromosome 1, Chromosome 14, Chromosome 12, Chromosome 6, Balancer chromosome, Sex chromosome, Chromosome instability, Chromosome 11, Y chromosome microdeletion, Chromosome 20, Chromosome regions, Chromosome 8, Chromosome 16, B chromosome, Chromosome 10, Chromosome 19, Chromosome condensation, Satellite chromosome, Polytene chromosome, Yeast artificial chromosome, Artificial chromosome, Ring chromosome 15, Chromosomal inversion, Small supernumerary marker chromosome, Ring chromosome 20 syndrome, Ring chromosome 14 syndrome, Chromosome territories, Chromosomal translocation, Boveri–Sutton chromosome theory, Ring chromosome 18, Homologous chromosome, Philadelphia chromosome, Ring chromosome 22, Chromosome (evolutionary algorithm), Eukaryotic chromosome structure, Chromosome 15q trisomy, Chromosome segregation, Ring chromosome, Human Y-chromosome DNA haplogroup, Y-chromosomal Adam, Sex chromosome anomalies, Y Chromosome Consortium, The Calcutta Chromosome, Human artificial chromosome, Chromosome 2q deletion, Sex-chromosome dosage compensation, Chromosome instability syndrome, Chromosome 15q partial deletion, Holocentric chromosome, Chromosomal rearrangement, Bacterial artificial chromosome, Chromosome conformation capture, Chromosome 1 open reading frame 194, Chromosomal deletion syndrome, Segmental duplication on the human Y chromosome, Chromosome engineering, Normalized chromosome value, Chromosomal fragile site, Monocentric chromosome, Derivative chromosome, Chromosome 2q31.1 duplication syndrome gene, Microcell-mediated chromosome transfer, List of organisms by chromosome count, Conversion table for Y chromosome haplogroups, Y-chromosomal Aaron, Chromosome X open reading frame 57, Chromosome jumping, Y Chromosome Haplotype Reference Database, Chromosome scaffold, Lampbrush chromosome, Karyotype, Dicentric chromosome, Marker chromosome, Trisomy 8, Chromosome 5q deletion syndrome, Isochromosome, Nondisjunction, Trisomy 16, XY sex-determination system, Chromosome 12 open reading frame 71, Polycentric chromosome, Linear chromosome, Chromosome No. 1 syndrome, X-inactivation, Parasitic chromosome, Premature chromosome condensation, ZW sex-determination system, Chromosome microdissection, Trisomy 22, Mosaic loss of chromosome Y, Secondary chromosome, Supernumerary chromosome, Trisomy 9, Autosome, Control of chromosome duplication, X-chromosome reactivation, Eukaryotic chromosome fine structure, List of Y-chromosome haplogroups in populations of the world, Aneuploidy, Chromosome landing, Ploidy, Bivalent (genetics), XYY syndrome, Chromosome combing, 3p deletion syndrome, Microfluidic whole genome haplotyping, Distal trisomy 10q, Trisomy 18, Chromosome 5 open reading frame 47, P1-derived artificial chromosome, Micronucleus, Isodicentric 15, C11orf91, Microchromosome, Cytogenetics, Centromere, C12orf54, Skewed X-inactivation, Chromosomal polymorphism, Monosomy 9p, Acentric fragment, Tetrasomy 9p, 2q37 deletion syndrome, Chromosome 21 open reading frame 91, Primer walking, Lists of human genes, Chromosome 21 (TV series), Genes, Chromosomes & Cancer, Double minute, Chromosome 11 open reading frame 80, Chromosome 9 open reading frame 116, C7orf26, Sister chromatids, SCZD11