Chromosome number

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

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

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