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

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

Chromosome, Chromosome abnormality, Y chromosome, Chromosome 2, X chromosome, Chromosome 21, Chromosome 17, Chromosome 13, Chromosome 7, Chromosome 4, Chromosome 9, Chromosome 18, Chromosome 5, Chromosome 15, Chromosome 22, Chromosome instability, Sex chromosome, Circular chromosome, Chromosome 12, Chromosome regions, Chromosome 1, Chromosome 11, Chromosome 3, Balancer chromosome, Chromosome 6, Chromosome 20, Chromosome 14, Chromosome 8, Chromosome 16, B chromosome, Chromosome 10, Chromosome 19, Polytene chromosome, Yeast artificial chromosome, Satellite chromosome, Ring chromosome 15, Ring chromosome 14 syndrome, Chromosomal inversion, Ring chromosome 20 syndrome, Chromosomal translocation, Y chromosome microdeletion, Artificial chromosome, Chromosome territories, Boveri–Sutton chromosome theory, Small supernumerary marker chromosome, Philadelphia chromosome, Ring chromosome 22, Ring chromosome 18, Homologous chromosome, Eukaryotic chromosome structure, Chromosome 15q trisomy, Human Y-chromosome DNA haplogroup, Chromosome (evolutionary algorithm), Ring chromosome, Chromosome segregation, Y-chromosomal Adam, Sex chromosome anomalies, Sex-chromosome dosage compensation, Chromosome 15q partial deletion, The Calcutta Chromosome, Chromosome 2q deletion, Human artificial chromosome, Y Chromosome Consortium, Holocentric chromosome, Chromosome instability syndrome, Bacterial artificial chromosome, Chromosomal rearrangement, Chromosome 1 open reading frame 194, Chromosome conformation capture, Segmental duplication on the human Y chromosome, Chromosomal deletion syndrome, Chromosome engineering, Normalized chromosome value, Chromosome 2q31.1 duplication syndrome gene, Chromosomal fragile site, Monocentric chromosome, Derivative chromosome, Chromosome X open reading frame 57, List of organisms by chromosome count, Chromosome jumping, Y-chromosomal Aaron, Microcell-mediated chromosome transfer, Chromosome scaffold, Lampbrush chromosome, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Karyotype, Marker chromosome, Dicentric chromosome, Trisomy 8, Nondisjunction, Chromosome 5q deletion syndrome, Isochromosome, XY sex-determination system, Trisomy 16, Trisomy 9, Polycentric chromosome, Chromosome No. 1 syndrome, Chromosome microdissection, X-inactivation, Chromosome 12 open reading frame 71, Linear chromosome, Premature chromosome condensation, Parasitic chromosome, Trisomy 22, Supernumerary chromosome, Secondary chromosome, Autosome, ZW sex-determination system, List of Y-chromosome haplogroups in populations of the world, Mosaic loss of chromosome Y, Control of chromosome duplication, Eukaryotic chromosome fine structure, X-chromosome reactivation, Bivalent (genetics), Aneuploidy, Chromosome landing, 3p deletion syndrome, XYY syndrome, Ploidy, Chromosome combing, P1-derived artificial chromosome, Microfluidic whole genome haplotyping, Distal trisomy 10q, Trisomy 18, C11orf91, Micronucleus, C12orf54, Isodicentric 15, Centromere, Microchromosome, Chromosomal polymorphism, Skewed X-inactivation, Monosomy 9p, Tetrasomy 9p, Cytogenetics, Chromosome 5 open reading frame 47, Acentric fragment, Lists of human genes, Chromosome 21 open reading frame 91, 2q37 deletion syndrome, Double minute, Primer walking, Chromosome 21 (TV series), Chromosome 11 open reading frame 80, Chromosome 9 open reading frame 116, C7orf26, SCZD11, Sister chromatids, Non-random segregation of chromosomes, Dup15q