Chromosome number

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

Chromosomal translocation, Chromosomal inversion, Boveri–Sutton chromosome theory, Small supernumerary marker chromosome, Chromosome territories, Y Chromosome Consortium, Ring chromosome 18, Homologous chromosome, Philadelphia chromosome, Ring chromosome 22, Eukaryotic chromosome structure, Chromosome (evolutionary algorithm), Chromosome segregation, Ring chromosome, Chromosome 15q trisomy, Y-chromosomal Adam, Sex chromosome anomalies, Human Y-chromosome DNA haplogroup, The Calcutta Chromosome, Sex-chromosome dosage compensation, Chromosome 15q partial deletion, Human artificial chromosome, Chromosome 2q deletion, Chromosome instability syndrome, Bacterial artificial chromosome, Chromosomal rearrangement, Holocentric chromosome, Chromosome 1 open reading frame 194, Chromosome conformation capture, Chromosomal deletion syndrome, Chromosome engineering, Segmental duplication on the human Y chromosome, Normalized chromosome value, Chromosome 2q31.1 duplication syndrome gene, Monocentric chromosome, Derivative chromosome, Chromosomal fragile site, 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, Karyotype, Marker chromosome, Y Chromosome Haplotype Reference Database, Dicentric chromosome, Trisomy 8

Chromosome, Chromosome abnormality, Y chromosome, Chromosome 2, X chromosome, Chromosome 13, Chromosome 17, Chromosome 21, Chromosome 4, Chromosome 5, Chromosome 15, Chromosome 7, Chromosome 9, Chromosome 18, Chromosome 22, Circular chromosome, Chromosome 3, Chromosome 11, Chromosome 1, Chromosome instability, Sex chromosome, Chromosome 12, Chromosome regions, Chromosome 6, Chromosome 14, Balancer chromosome, Chromosome 16, Y chromosome microdeletion, Chromosome 10, Chromosome 8, Chromosome 20, Yeast artificial chromosome, B chromosome, Polytene chromosome, Chromosome 19, Satellite chromosome, Chromosome condensation, Ring chromosome 15, Ring chromosome 14 syndrome, Artificial chromosome, Ring chromosome 20 syndrome, Chromosomal translocation, Chromosomal inversion, Boveri–Sutton chromosome theory, Small supernumerary marker chromosome, Chromosome territories, Y Chromosome Consortium, Ring chromosome 18, Homologous chromosome, Philadelphia chromosome, Ring chromosome 22, Eukaryotic chromosome structure, Chromosome (evolutionary algorithm), Chromosome segregation, Ring chromosome, Chromosome 15q trisomy, Y-chromosomal Adam, Sex chromosome anomalies, Human Y-chromosome DNA haplogroup, The Calcutta Chromosome, Sex-chromosome dosage compensation, Chromosome 15q partial deletion, Human artificial chromosome, Chromosome 2q deletion, Chromosome instability syndrome, Bacterial artificial chromosome, Chromosomal rearrangement, Holocentric chromosome, Chromosome 1 open reading frame 194, Chromosome conformation capture, Chromosomal deletion syndrome, Chromosome engineering, Segmental duplication on the human Y chromosome, Normalized chromosome value, Chromosome 2q31.1 duplication syndrome gene, Monocentric chromosome, Derivative chromosome, Chromosomal fragile site, 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, Karyotype, Marker chromosome, Y Chromosome Haplotype Reference Database, Dicentric chromosome, Trisomy 8, Chromosome 5q deletion syndrome, Nondisjunction, Isochromosome, Trisomy 16, XY sex-determination system, Chromosome 12 open reading frame 71, Chromosome No. 1 syndrome, Polycentric chromosome, X-inactivation, Premature chromosome condensation, Linear chromosome, Chromosome microdissection, Parasitic chromosome, Mosaic loss of chromosome Y, ZW sex-determination system, Trisomy 9, Supernumerary chromosome, Trisomy 22, Autosome, Secondary chromosome, List of Y-chromosome haplogroups in populations of the world, X-chromosome reactivation, Eukaryotic chromosome fine structure, Chromosome landing, Ploidy, Aneuploidy, Control of chromosome duplication, Bivalent (genetics), XYY syndrome, Distal trisomy 10q, Microfluidic whole genome haplotyping, Trisomy 18, Chromosome combing, 3p deletion syndrome, Micronucleus, Isodicentric 15, P1-derived artificial chromosome, Centromere, C11orf91, Chromosome 5 open reading frame 47, Cytogenetics, C12orf54, Monosomy 9p, Skewed X-inactivation, Chromosomal polymorphism, Tetrasomy 9p, Acentric fragment, Microchromosome, Chromosome 21 open reading frame 91, Lists of human genes, 2q37 deletion syndrome, Genes, Chromosomes & Cancer, Chromosome 21 (TV series), Primer walking, Double minute, Chromosome 11 open reading frame 80, C7orf26, Chromosome 9 open reading frame 116, Sister chromatids, Chromosome 9 open reading frame 135