Chromosome 8 (human)

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

Chromosomal inversion, Chromosomal translocation, 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), Chromosome 15q trisomy, Y-chromosomal Adam, Sex chromosome anomalies, 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, Holocentric chromosome, Chromosome instability syndrome, Chromosome 1 open reading frame 194, Chromosomal rearrangement, Chromosome conformation capture, Chromosomal deletion syndrome, Chromosome engineering, Segmental duplication on the human Y chromosome, Normalized chromosome value, Chromosome 2q31.1 duplication syndrome gene, Derivative chromosome, Chromosomal fragile site, Monocentric chromosome, Chromosome X open reading frame 57, Y-chromosomal Aaron, Microcell-mediated chromosome transfer, List of organisms by chromosome count, Chromosome jumping, Chromosome scaffold, Lampbrush chromosome, Conversion table for Y chromosome haplogroups, Y Chromosome Haplotype Reference Database, Marker chromosome, Karyotype, Dicentric chromosome, Trisomy 8

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