Chromosome, Chromosome 2, Chromosome abnormality, Y chromosome, X chromosome, Chromosome 21, Chromosome 13, Chromosome 17, Chromosome 5, Chromosome 15, Chromosome 7, Chromosome 9, Chromosome 4, Chromosome 18, Circular chromosome, Chromosome 22, Chromosome instability, Sex chromosome, Chromosome 12, Chromosome 11, Chromosome 1, Chromosome regions, Balancer chromosome, Chromosome 3, Chromosome 6, Chromosome 20, Chromosome 14, Chromosome 8, Chromosome 16, B chromosome, Chromosome 10, Chromosome 19, Yeast artificial chromosome, Polytene 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, Ring chromosome 18, Philadelphia chromosome, Ring chromosome 22, Homologous chromosome, Eukaryotic chromosome structure, Ring chromosome, Chromosome segregation, Chromosome 15q trisomy, Y-chromosomal Adam, Human Y-chromosome DNA haplogroup, Sex chromosome anomalies, Chromosome (evolutionary algorithm), The Calcutta Chromosome, Sex-chromosome dosage compensation, Chromosome 15q partial deletion, Chromosome 2q deletion, Human artificial chromosome, Y Chromosome Consortium, Holocentric chromosome, Bacterial artificial chromosome, Chromosome instability syndrome, Chromosomal rearrangement, Chromosome conformation capture, Chromosome 1 open reading frame 194, Chromosomal deletion syndrome, Segmental duplication on the human Y chromosome, 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, Microcell-mediated chromosome transfer, Chromosome jumping, Chromosome scaffold, Lampbrush chromosome, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Karyotype, Marker chromosome, Y-chromosomal Aaron, Dicentric chromosome, Trisomy 8, Nondisjunction

Chromosome, Chromosome 2, Chromosome abnormality, Y chromosome, X chromosome, Chromosome 21, Chromosome 13, Chromosome 17, Chromosome 5, Chromosome 15, Chromosome 7, Chromosome 9, Chromosome 4, Chromosome 18, Circular chromosome, Chromosome 22, Chromosome instability, Sex chromosome, Chromosome 12, Chromosome 11, Chromosome 1, Chromosome regions, Balancer chromosome, Chromosome 3, Chromosome 6, Chromosome 20, Chromosome 14, Chromosome 8, Chromosome 16, B chromosome, Chromosome 10, Chromosome 19, Yeast artificial chromosome, Polytene 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, Ring chromosome 18, Philadelphia chromosome, Ring chromosome 22, Homologous chromosome, Eukaryotic chromosome structure, Ring chromosome, Chromosome segregation, Chromosome 15q trisomy, Y-chromosomal Adam, Human Y-chromosome DNA haplogroup, Sex chromosome anomalies, Chromosome (evolutionary algorithm), The Calcutta Chromosome, Sex-chromosome dosage compensation, Chromosome 15q partial deletion, Chromosome 2q deletion, Human artificial chromosome, Y Chromosome Consortium, Holocentric chromosome, Bacterial artificial chromosome, Chromosome instability syndrome, Chromosomal rearrangement, Chromosome conformation capture, Chromosome 1 open reading frame 194, Chromosomal deletion syndrome, Segmental duplication on the human Y chromosome, 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, Microcell-mediated chromosome transfer, Chromosome jumping, Chromosome scaffold, Lampbrush chromosome, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Karyotype, Marker chromosome, Y-chromosomal Aaron, Dicentric chromosome, Trisomy 8, Nondisjunction, Chromosome 5q deletion syndrome, Isochromosome, Trisomy 16, Trisomy 9, XY sex-determination system, Polycentric chromosome, Chromosome No. 1 syndrome, Chromosome microdissection, X-inactivation, Chromosome 12 open reading frame 71, Premature chromosome condensation, Linear chromosome, Parasitic chromosome, Trisomy 22, Supernumerary chromosome, ZW sex-determination system, Secondary chromosome, Autosome, Mosaic loss of chromosome Y, Eukaryotic chromosome fine structure, Bivalent (genetics), Control of chromosome duplication, List of Y-chromosome haplogroups in populations of the world, X-chromosome reactivation, Aneuploidy, Chromosome landing, 3p deletion syndrome, XYY syndrome, Ploidy, Distal trisomy 10q, P1-derived artificial chromosome, Trisomy 18, Microfluidic whole genome haplotyping, Chromosome combing, Isodicentric 15, Micronucleus, Centromere, Microchromosome, C11orf91, C12orf54, Cytogenetics, Monosomy 9p, Skewed X-inactivation, Tetrasomy 9p, Chromosomal polymorphism, Acentric fragment, Lists of human genes, Chromosome 5 open reading frame 47, Chromosome 21 open reading frame 91, Double minute, 2q37 deletion syndrome, Primer walking, Chromosome 11 open reading frame 80, Chromosome 21 (TV series), C7orf26, SCZD11, Sister chromatids, Chromosome 9 open reading frame 116, Chromosome 9 open reading frame 135, 13q deletion syndrome