Chromosome
Chromosome abnormality
Chromosome 2
Y chromosome
X chromosome
Chromosome 21
Chromosome 13
Chromosome 5
Chromosome 15
Chromosome 17
Chromosome 7
Chromosome 9
Chromosome 18
Chromosome 4
Chromosome 22
Chromosome instability
Sex chromosome
Chromosome regions
Chromosome 1
Circular chromosome
Chromosome 3
Chromosome 12
Chromosome 6
Chromosome 11
Chromosome 14
Balancer chromosome
Chromosome 20
Chromosome 8
Chromosome 16
B chromosome
Yeast artificial chromosome
Satellite chromosome
Chromosome 19
Chromosome 10
Polytene chromosome
Ring chromosome 15
Ring chromosome 14 syndrome
Chromosomal inversion
Y chromosome microdeletion
Artificial chromosome
Chromosomal translocation
Ring chromosome 20 syndrome
Boveri–Sutton chromosome theory
Chromosome territories
Philadelphia chromosome
Small supernumerary marker chromosome
Homologous chromosome
Ring chromosome 22
Ring chromosome 18
Eukaryotic chromosome structure
Chromosome 15q trisomy
Ring chromosome
Chromosome (evolutionary algorithm)
Chromosome segregation
Sex-chromosome dosage compensation
Y-chromosomal Adam
Sex chromosome anomalies
Human Y-chromosome DNA haplogroup
Chromosome 15q partial deletion
Chromosome 2q deletion
Y Chromosome Consortium
Human artificial chromosome
The Calcutta Chromosome
Holocentric chromosome
Chromosomal rearrangement
Chromosome instability syndrome
Bacterial artificial chromosome
Chromosome 1 open reading frame 194
Chromosome conformation capture
Chromosome engineering
Segmental duplication on the human Y chromosome
Chromosomal deletion syndrome
Normalized chromosome value
Chromosome 2q31.1 duplication syndrome gene
Chromosomal fragile site
Derivative chromosome
Monocentric chromosome
Chromosome jumping
Chromosome X open reading frame 57
Chromosome scaffold
Microcell-mediated chromosome transfer
Lampbrush chromosome
List of organisms by chromosome count
Conversion table for Y chromosome haplogroups
Y Chromosome Haplotype Reference Database
Y-chromosomal Aaron
Karyotype
Marker chromosome
Dicentric chromosome
Trisomy 8
Chromosome 5q deletion syndrome
Nondisjunction
Isochromosome
Trisomy 16
XY sex-determination system
Trisomy 9
Polycentric chromosome
Chromosome microdissection
Chromosome No. 1 syndrome
Premature chromosome condensation
Chromosome 12 open reading frame 71
Linear chromosome
X-inactivation
Parasitic chromosome
Trisomy 22
Supernumerary chromosome
Secondary chromosome
ZW sex-determination system
Mosaic loss of chromosome Y
Autosome
List of Y-chromosome haplogroups in populations of the world
X-chromosome reactivation
Chromosome landing
Aneuploidy
Control of chromosome duplication
Bivalent (genetics)
3p deletion syndrome
Microfluidic whole genome haplotyping
XYY syndrome
P1-derived artificial chromosome
Distal trisomy 10q
Eukaryotic chromosome fine structure
Micronucleus
Trisomy 18
Chromosome combing
Isodicentric 15
Centromere
Microchromosome
Skewed X-inactivation
C11orf91
Cytogenetics
Chromosomal polymorphism
C12orf54
Tetrasomy 9p
Monosomy 9p
Ploidy
Chromosome 5 open reading frame 47
Acentric fragment
Lists of human genes
Chromosome 21 open reading frame 91
2q37 deletion syndrome
Primer walking
Chromosome 11 open reading frame 80
Double minute
Chromosome 21 (TV series)
Chromosome 9 open reading frame 116
SCZD11
Sister chromatids
Non-random segregation of chromosomes
Chromosome 9 open reading frame 135
13q deletion syndrome
C7orf26
Trisomy
Chromosome 6 open reading frame 203
Genes, Chromosomes & Cancer
Chromosome 17 open reading frame 67
Chromosome 4 open reading frame 50
Chromosomal crossover
Locus (genetics)
Chromosome 1 open reading frame 162
Tetrasomy 18p
Chromosome 4 open reading frame 54
Gene duplication
C19orf44
Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer
HIKESHI
Polycomb recruitment in X chromosome inactivation
C5orf52
Chromosome 20 open reading frame 85
1p36 deletion syndrome
Fluorescence in situ hybridization
Jacobsen syndrome
Allregulin
METTL26
Chromosome 19 open reading frame 33
Dup15q
Wolf–Hirschhorn syndrome
C13orf16
Deletion (genetics)
Thymosin beta-4, Y-chromosomal
DiGeorge syndrome
2q37 monosomy
Frontotemporal dementia and parkinsonism linked to chromosome 17
C21orf58
C9orf50
Cell division
C17orf75
18p-
Turner syndrome
Mosaic (genetics)
C19orf22
C16orf71
C19orf18
C15orf61
Smith–Magenis syndrome
Chromosome 9 open reading frame 43
CFAP206
C1orf112
Sex linkage
Meiosis