Chromosome number

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

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

Chromosome, Y chromosome, Chromosome abnormality, Chromosome 2, Chromosome 13, X chromosome, Chromosome 21, Chromosome 5, Chromosome 15, Chromosome 7, Chromosome 17, Chromosome 9, Chromosome 18, Chromosome 4, Chromosome 22, Chromosome 3, Chromosome instability, Sex chromosome, Chromosome 1, Chromosome regions, Circular chromosome, Chromosome 14, Chromosome 6, Chromosome 11, Chromosome 12, Chromosome 16, Chromosome 8, Balancer chromosome, Chromosome 20, Chromosome 10, B chromosome, Chromosome 19, Satellite chromosome, Chromosome condensation, Yeast artificial chromosome, Polytene chromosome, Ring chromosome 15, Y chromosome microdeletion, Artificial chromosome, Chromosomal inversion, Chromosomal translocation, Ring chromosome 14 syndrome, Boveri–Sutton chromosome theory, Ring chromosome 20 syndrome, Small supernumerary marker chromosome, Chromosome territories, Ring chromosome 18, Homologous chromosome, Philadelphia chromosome, Ring chromosome 22, Chromosome (evolutionary algorithm), Eukaryotic chromosome structure, Chromosome segregation, Ring chromosome, Chromosome 15q trisomy, Human Y-chromosome DNA haplogroup, The Calcutta Chromosome, Y-chromosomal Adam, Sex-chromosome dosage compensation, Sex chromosome anomalies, Human artificial chromosome, Chromosome 2q deletion, Y Chromosome Consortium, Chromosome 15q partial deletion, Chromosome instability syndrome, Holocentric chromosome, Bacterial artificial chromosome, Chromosomal rearrangement, Chromosome conformation capture, Chromosomal deletion syndrome, Chromosome 1 open reading frame 194, Segmental duplication on the human Y chromosome, Chromosome engineering, Chromosomal fragile site, Normalized chromosome value, Monocentric chromosome, Chromosome 2q31.1 duplication syndrome gene, Microcell-mediated chromosome transfer, Derivative chromosome, Chromosome scaffold, Lampbrush chromosome, Conversion table for Y chromosome haplogroups, Chromosome X open reading frame 57, List of organisms by chromosome count, Chromosome jumping, Y Chromosome Haplotype Reference Database, Y-chromosomal Aaron, Karyotype, Dicentric chromosome, Marker chromosome, Trisomy 8, Nondisjunction, Chromosome 5q deletion syndrome, Isochromosome, Trisomy 16, XY sex-determination system, Chromosome 12 open reading frame 71, Polycentric chromosome, Trisomy 9, X-inactivation, Chromosome No. 1 syndrome, Premature chromosome condensation, Linear chromosome, Chromosome microdissection, Parasitic chromosome, ZW sex-determination system, Mosaic loss of chromosome Y, Trisomy 22, Secondary chromosome, Autosome, Supernumerary chromosome, Eukaryotic chromosome fine structure, List of Y-chromosome haplogroups in populations of the world, Control of chromosome duplication, Bivalent (genetics), X-chromosome reactivation, Chromosome landing, Aneuploidy, Ploidy, Distal trisomy 10q, 3p deletion syndrome, Trisomy 18, Microfluidic whole genome haplotyping, Chromosome combing, XYY syndrome, P1-derived artificial chromosome, Isodicentric 15, Micronucleus, Cytogenetics, Chromosome 5 open reading frame 47, Centromere, Microchromosome, Skewed X-inactivation, Acentric fragment, C12orf54, C11orf91, Tetrasomy 9p, Monosomy 9p, Chromosomal polymorphism, Chromosome 21 open reading frame 91, Primer walking, Lists of human genes, 2q37 deletion syndrome, Double minute, Chromosome 11 open reading frame 80, Chromosome 21 (TV series), C7orf26, Sister chromatids, Chromosome 9 open reading frame 116, Chromosome 9 open reading frame 135, Dup15q