Chromosome anomaly

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

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

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