Chromosome five

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

Ring chromosome 20 syndrome, Chromosomal translocation, Small supernumerary marker chromosome, Chromosome territories, Boveri–Sutton chromosome theory, Y Chromosome Consortium, Ring chromosome 18, Philadelphia chromosome, Homologous chromosome, Ring chromosome 22, Eukaryotic chromosome structure, Chromosome (evolutionary algorithm), Chromosome segregation, Ring chromosome, Chromosome 15q trisomy, The Calcutta Chromosome, Human Y-chromosome DNA haplogroup, Sex chromosome anomalies, Y-chromosomal Adam, Human artificial chromosome, Chromosome 2q deletion, Chromosome 15q partial deletion, Sex-chromosome dosage compensation, Chromosome instability syndrome, Holocentric chromosome, Bacterial artificial chromosome, Chromosome conformation capture, Chromosomal rearrangement, Chromosome 1 open reading frame 194, Chromosomal deletion syndrome, Chromosome engineering, Segmental duplication on the human Y chromosome, Normalized chromosome value, Monocentric chromosome, Chromosome 2q31.1 duplication syndrome gene, Chromosomal fragile site, Derivative chromosome, Microcell-mediated chromosome transfer, Y-chromosomal Aaron, Chromosome jumping, Chromosome X open reading frame 57, Chromosome scaffold, Lampbrush chromosome, List of organisms by chromosome count, Y Chromosome Haplotype Reference Database, Conversion table for Y chromosome haplogroups, Dicentric chromosome, Marker chromosome, Karyotype, Chromosome 5q deletion syndrome

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