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