Chromosome 3 (human)

Chromosome, Chromosome abnormality, Y chromosome, Chromosome 2, X chromosome, Chromosome 13, Chromosome 17, Chromosome 5, Chromosome 21, Chromosome 15, Chromosome 4, Chromosome 7, Chromosome 9, Chromosome 18, Chromosome 22, Circular chromosome, Chromosome 11, Chromosome 12, Chromosome 3, Chromosome instability, Chromosome 1, Sex chromosome, Chromosome regions, Chromosome 6, Balancer chromosome, Chromosome 14, Chromosome 16, Chromosome 8, Chromosome 10, Chromosome 20, Y chromosome microdeletion, B chromosome, Chromosome 19, Yeast artificial chromosome, Polytene chromosome, Satellite chromosome, Chromosome condensation, Ring chromosome 14 syndrome, Ring chromosome 15, 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), Y-chromosomal Adam, Sex chromosome anomalies, Chromosome 15q trisomy, The Calcutta Chromosome, Chromosome 15q partial deletion, Sex-chromosome dosage compensation, Human Y-chromosome DNA haplogroup, Human artificial chromosome, Chromosome 2q deletion, Holocentric chromosome, Bacterial artificial chromosome, Chromosome instability syndrome, Chromosome 1 open reading frame 194, Chromosomal rearrangement, Chromosome conformation capture, Chromosomal deletion syndrome, Segmental duplication on the human Y chromosome, Chromosome engineering, Normalized chromosome value, Chromosome 2q31.1 duplication syndrome gene, Chromosomal fragile site, Monocentric chromosome, Derivative chromosome, Chromosome X open reading frame 57, Microcell-mediated chromosome transfer, Chromosome jumping, List of organisms by chromosome count, Y-chromosomal Aaron, Chromosome scaffold, Lampbrush chromosome, Y Chromosome Haplotype Reference Database, Conversion table for Y chromosome haplogroups, Marker chromosome, Karyotype, Dicentric chromosome, Trisomy 8

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