Chromosome, Y chromosome, Chromosome abnormality, Chromosome 2, X chromosome, Chromosome 21, Chromosome 13, Chromosome 17, Chromosome 7, Chromosome 4, Chromosome 9, Chromosome 18, Chromosome 5, Chromosome 15, Chromosome 22, Chromosome instability, Sex chromosome, Circular chromosome, Chromosome 3, Chromosome 12, Chromosome regions, Chromosome 1, Chromosome 11, Balancer chromosome, Chromosome 6, Chromosome 14, Chromosome 20, 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, Y chromosome microdeletion, Chromosomal translocation, Ring chromosome 20 syndrome
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 (evolutionary algorithm), Chromosome 15q trisomy, Human Y-chromosome DNA haplogroup, 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, Microcell-mediated chromosome transfer, Chromosome scaffold, Lampbrush chromosome, Y-chromosomal Aaron, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Marker chromosome, Karyotype, Dicentric chromosome, Trisomy 8, Nondisjunction
Chromosome, Y chromosome, Chromosome abnormality, Chromosome 2, X chromosome, Chromosome 21, Chromosome 13, Chromosome 17, Chromosome 7, Chromosome 4, Chromosome 9, Chromosome 18, Chromosome 5, Chromosome 15, Chromosome 22, Chromosome instability, Sex chromosome, Circular chromosome, Chromosome 3, Chromosome 12, Chromosome regions, Chromosome 1, Chromosome 11, Balancer chromosome, Chromosome 6, Chromosome 14, Chromosome 20, 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, Y chromosome microdeletion, Chromosomal translocation, Ring chromosome 20 syndrome, 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 (evolutionary algorithm), Chromosome 15q trisomy, Human Y-chromosome DNA haplogroup, 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, Microcell-mediated chromosome transfer, Chromosome scaffold, Lampbrush chromosome, Y-chromosomal Aaron, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Marker chromosome, Karyotype, 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, ZW sex-determination system, Autosome, Mosaic loss of chromosome Y, List of Y-chromosome haplogroups in populations of the world, 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, Distal trisomy 10q, Microfluidic whole genome haplotyping, Trisomy 18, Micronucleus, Isodicentric 15, C11orf91, Centromere, Microchromosome, C12orf54, Chromosomal polymorphism, Skewed X-inactivation, Monosomy 9p, Tetrasomy 9p, Chromosome 5 open reading frame 47, Cytogenetics, Acentric fragment, Lists of human genes, Chromosome 21 open reading frame 91, Primer walking, Double minute, 2q37 deletion syndrome, 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, 13q deletion syndrome