Chromosome translocation

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

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

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