Chromosome, Chromosome abnormality, Chromosomal inversion, Chromosomal translocation, Y-chromosomal Adam, Chromosome instability, Y chromosome, Chromosomal rearrangement, Chromosome 13, Chromosomal deletion syndrome, Chromosome instability syndrome, Polytene chromosome, Satellite chromosome, Chromosome 15, Chromosome 2, Balancer chromosome, Chromosome 22, Chromosome 5, Y-chromosomal Aaron, Chromosome 21, Circular chromosome, Homologous chromosome, X chromosome, Chromosome segregation, Chromosome 7, Holocentric chromosome, B chromosome, Chromosomal fragile site, Chromosomal polymorphism, Ring chromosome 20 syndrome, Chromosome regions, Small supernumerary marker chromosome, Chromosome 17, Sex chromosome, Chromosome 6, Ring chromosome 22, Chromosome 4, Human Y-chromosome DNA haplogroup, Y Chromosome Consortium, Chromosome condensation, Chromosome 15q partial deletion

Chromosome 9, Chromosome 18, Chromosome 3, Chromosome 1, Chromosome 14, Chromosome 12, Chromosome engineering, Chromosome 20, Philadelphia chromosome, Chromosome 11, Chromosome 8, Eukaryotic chromosome structure, Y chromosome microdeletion, Yeast artificial chromosome, Chromosome 19, Chromosome 16, Chromosome 10, Chromosome conformation capture, Ring chromosome 14 syndrome, Artificial chromosome, Boveri–Sutton chromosome theory, Sex chromosome anomalies, Ring chromosome 15, Segmental duplication on the human Y chromosome, List of organisms by chromosome count, Normalized chromosome value, Chromosomal crossover, Ring chromosome, Nondisjunction, Chromosome territories, Karyotype, Y Chromosome Haplotype Reference Database, Ring chromosome 18, Dicentric chromosome, Chromosome (evolutionary algorithm), Sex-chromosome dosage compensation, Conversion table for Y chromosome haplogroups, Trisomy 16, Cytogenetics, Chromosome 15q trisomy, Human artificial chromosome, Aneuploidy, The Calcutta Chromosome, Trisomy 8, Genes, Chromosomes & Cancer, Bacterial artificial chromosome, Thymosin beta-4, Y-chromosomal, Chromosome 2q deletion, Chromosome No. 1 syndrome, Chromosome jumping

Chromosome, Chromosome abnormality, Chromosomal inversion, Chromosomal translocation, Y-chromosomal Adam, Chromosome instability, Y chromosome, Chromosomal rearrangement, Chromosome 13, Chromosomal deletion syndrome, Chromosome instability syndrome, Polytene chromosome, Satellite chromosome, Chromosome 15, Chromosome 2, Balancer chromosome, Chromosome 22, Chromosome 5, Y-chromosomal Aaron, Chromosome 21, Circular chromosome, Homologous chromosome, X chromosome, Chromosome segregation, Chromosome 7, Holocentric chromosome, B chromosome, Chromosomal fragile site, Chromosomal polymorphism, Ring chromosome 20 syndrome, Chromosome regions, Small supernumerary marker chromosome, Chromosome 17, Sex chromosome, Chromosome 6, Ring chromosome 22, Chromosome 4, Human Y-chromosome DNA haplogroup, Y Chromosome Consortium, Chromosome condensation, Chromosome 15q partial deletion, Chromosome 9, Chromosome 18, Chromosome 3, Chromosome 1, Chromosome 14, Chromosome 12, Chromosome engineering, Chromosome 20, Philadelphia chromosome, Chromosome 11, Chromosome 8, Eukaryotic chromosome structure, Y chromosome microdeletion, Yeast artificial chromosome, Chromosome 19, Chromosome 16, Chromosome 10, Chromosome conformation capture, Ring chromosome 14 syndrome, Artificial chromosome, Boveri–Sutton chromosome theory, Sex chromosome anomalies, Ring chromosome 15, Segmental duplication on the human Y chromosome, List of organisms by chromosome count, Normalized chromosome value, Chromosomal crossover, Ring chromosome, Nondisjunction, Chromosome territories, Karyotype, Y Chromosome Haplotype Reference Database, Ring chromosome 18, Dicentric chromosome, Chromosome (evolutionary algorithm), Sex-chromosome dosage compensation, Conversion table for Y chromosome haplogroups, Trisomy 16, Cytogenetics, Chromosome 15q trisomy, Human artificial chromosome, Aneuploidy, The Calcutta Chromosome, Trisomy 8, Genes, Chromosomes & Cancer, Bacterial artificial chromosome, Thymosin beta-4, Y-chromosomal, Chromosome 2q deletion, Chromosome No. 1 syndrome, Chromosome jumping, Chromosome 12 open reading frame 71, Polycentric chromosome, ZW sex-determination system, Distal trisomy 10q, Trisomy, Micronucleus, Gene duplication, Isochromosome, 3p deletion syndrome, Chromosome 1 open reading frame 194, Trisomy 9, XY sex-determination system, Deletion (genetics), Autosome, X-inactivation, Primer walking, Trisomy 22, Chromosome landing, Centromere, Monosomy 9p, Tetrasomy 9p, Chromosome microdissection, Monocentric chromosome, Microcell-mediated chromosome transfer, Double minute, Isodicentric 15, Chromosome 2q31.1 duplication syndrome gene, DECIPHER, Mosaic (genetics), Chromosome X open reading frame 57, Trisomy 18, Eukaryotic chromosome fine structure, Chromosome 5q deletion syndrome, Locus (genetics), XYY syndrome, Marker chromosome, Derivative chromosome, Non-random segregation of chromosomes, Comparative genomic hybridization, Lampbrush chromosome, Microchromosome, Chromosome scaffold, Ploidy, Control of chromosome duplication, Fluorescence in situ hybridization, Bivalent (genetics), 1p36 deletion syndrome, List of Y-chromosome haplogroups in populations of the world, Secondary chromosome, Wolf–Hirschhorn syndrome, Linear chromosome, Dup15q, Premature chromosome condensation, Cell division, Parasitic chromosome, Jacobsen syndrome, Microfluidic whole genome haplotyping, C5orf52, DiGeorge syndrome, Mosaic loss of chromosome Y