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