Chromosome
Chromosome abnormality
Chromosome 2
Y chromosome
Chromosome 13
X chromosome
Chromosome 21
Chromosome 17
Chromosome 5
Chromosome 15
Chromosome 4
Chromosome 7
Chromosome 22
Chromosome 9
Chromosome 18
Chromosome instability
Sex chromosome
Chromosome 1
Chromosome 3
Chromosome regions
Circular chromosome
Chromosome 6
Chromosome 12
Chromosome 14
Chromosome 11
Balancer chromosome
Chromosome 20
Chromosome 16
Chromosome 8
B chromosome
Satellite chromosome
Yeast artificial chromosome
Chromosome 10
Chromosome 19
Polytene chromosome
Y chromosome microdeletion
Ring chromosome 15
Ring chromosome 14 syndrome
Artificial chromosome
Chromosomal inversion
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
Chromosome (evolutionary algorithm)
Ring chromosome
Chromosome segregation
Sex-chromosome dosage compensation
Y-chromosomal Adam
Sex chromosome anomalies
Chromosome 15q partial deletion
Human Y-chromosome DNA haplogroup
Y Chromosome Consortium
Chromosome 2q deletion
The Calcutta Chromosome
Human artificial chromosome
Chromosomal rearrangement
Holocentric chromosome
Chromosome instability syndrome
Bacterial artificial chromosome
Chromosome 1 open reading frame 194
Chromosome conformation capture
Chromosome engineering
Chromosomal deletion syndrome
Segmental duplication on the human Y chromosome
Normalized chromosome value
Chromosome 2q31.1 duplication syndrome gene
Derivative chromosome
Monocentric chromosome
Chromosomal fragile site
Chromosome jumping
Chromosome X open reading frame 57
Microcell-mediated chromosome transfer
Chromosome scaffold
Conversion table for Y chromosome haplogroups
Lampbrush chromosome
List of organisms by chromosome count
Y-chromosomal Aaron
Karyotype
Marker chromosome
Y Chromosome Haplotype Reference Database
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
ZW sex-determination system
Secondary chromosome
Mosaic loss of chromosome Y
Autosome
List of Y-chromosome haplogroups in populations of the world
X-chromosome reactivation
Chromosome landing
Bivalent (genetics)
Aneuploidy
Control of chromosome duplication
Microfluidic whole genome haplotyping
3p deletion syndrome
XYY syndrome
Distal trisomy 10q
P1-derived artificial chromosome
Micronucleus
Chromosome combing
Eukaryotic chromosome fine structure
Trisomy 18
Isodicentric 15
Centromere
Microchromosome
C11orf91
Chromosomal polymorphism
Cytogenetics
C12orf54
Tetrasomy 9p
Skewed X-inactivation
Ploidy
Chromosome 5 open reading frame 47
Monosomy 9p
Acentric fragment
Lists of human genes
Chromosome 21 open reading frame 91
Primer walking
2q37 deletion syndrome
Chromosome 11 open reading frame 80
Chromosome 9 open reading frame 116
Double minute
Chromosome 21 (TV series)
SCZD11
Sister chromatids
Non-random segregation of chromosomes
Chromosome 9 open reading frame 135
C7orf26
Trisomy
13q deletion syndrome
Chromosome 6 open reading frame 203
Chromosome 4 open reading frame 50
Genes, Chromosomes & Cancer
Chromosome 17 open reading frame 67
Chromosomal crossover
Locus (genetics)
Chromosome 1 open reading frame 162
Tetrasomy 18p
Chromosome 4 open reading frame 54
Gene duplication
C19orf44
HIKESHI
Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer
Chromosome 20 open reading frame 85
Polycomb recruitment in X chromosome inactivation
C5orf52
Fluorescence in situ hybridization
1p36 deletion syndrome
Jacobsen syndrome
Allregulin
METTL26
Chromosome 19 open reading frame 33
Dup15q
Wolf–Hirschhorn syndrome
C13orf16
Deletion (genetics)
Thymosin beta-4, Y-chromosomal
DiGeorge syndrome
Frontotemporal dementia and parkinsonism linked to chromosome 17
2q37 monosomy
C21orf58
C9orf50
Cell division
C17orf75
18p-
Turner syndrome
Mosaic (genetics)
C19orf18
C19orf22
C16orf71
C15orf61
Smith–Magenis syndrome
Chromosome 9 open reading frame 43
CFAP206
C1orf112
Sex linkage
C22orf23