Pages that link to "Chromosome 22 (human)"
The following pages link to Chromosome 22 (human):
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Autosome (← links)
- Chromosome (← links)
- Centromere (← links)
- Down syndrome (← links)
- Mutation (← links)
- XYY syndrome (← links)
- Trisomy (← links)
- Human genome (← links)
- Turner syndrome (← links)
- Fragile X syndrome (← links)
- Prader–Willi syndrome (← links)
- Thymus (← links)
- Karyotype (← links)
- X chromosome (← links)
- Williams syndrome (← links)
- TAR syndrome (← links)
- Deletion (genetics) (← links)
- Y chromosome (← links)
- Multiple myeloma (← links)
- Aneuploidy (← links)
- Jacobsen syndrome (← links)
- Congenital disorder (← links)
- Sterol regulatory element-binding protein (← links)
- XXYY syndrome (← links)
- Gamma-glutamyl transpeptidase (← links)
- Uniparental disomy (← links)
- Burkitt's lymphoma (← links)
- 22q13 deletion syndrome (← links)
- Isochromosome (← links)
- Smith–Magenis syndrome (← links)
- Clathrin (← links)
- Philadelphia chromosome (← links)
- Human β-globin locus (← links)
- MN1 (gene) (← links)
- Chromosomal translocation (← links)
- Trisomy 8 (← links)
- Peroxisome proliferator-activated receptor (← links)
- Mantle cell lymphoma (← links)
- Chromosome abnormality (← links)
- Human chromosome 22 (redirect page) (← links)
- CSNK1E (← links)
- MAPK11 (← links)
- DGCR8 (← links)
- DNAL4 (← links)
- KDELR3 (← links)
- DUSP18 (← links)
- SEZ6L (← links)
- TSSK2 (← links)
- APOL2 (← links)
- TMEM184B (← links)
- GGTLA1 (← links)
- PIB5PA (← links)
- CYTH4 (← links)
- CTA-126B4.3 (← links)
- MCAT (gene) (← links)
- MPST (← links)
- UPB1 (← links)
- NOL12 (← links)
- THAP7 (← links)
- LZTR1 (← links)
- KREMEN1 (← links)
- TUBGCP6 (← links)
- RAB36 (← links)
- Category:Human chromosome 22 gene stubs (← links)
- Template:Gene-22-stub (← links)
- SLC5A4 (← links)
- AP1B1 (← links)
- EIF3D (← links)
- LIMK2 (← links)
- MCM5 (← links)
- MKL1 (← links)
- MYO18B (← links)
- Nucleoporin 50 (← links)
- PATZ1 (← links)
- PMM1 (← links)
- PPIL2 (← links)
- RASD2 (← links)
- RBM9 (← links)
- SFI1 (← links)
- SLC2A11 (← links)
- SNRPD3 (← links)
- SYN3 (← links)
- TRIOBP (← links)
- ZNF74 (← links)
- ECGF1 (← links)
- CENPM (← links)
- CRYBA4 (← links)
- CRYBB3 (← links)
- CRYBB1 (← links)
- SHANK3 (← links)
- MAPK13 (← links)
- PDGFB (← links)
- MAPK12 (← links)
- HIC2 (← links)
- Heparin cofactor II (← links)
- List of congenital disorders (← links)
- Neurofibromatosis type II (← links)
- Infogalactic:WikiProject Molecular and Cell Biology/Style guidelines (← links)
- Trisomy 9 (← links)
- Beckwith–Wiedemann syndrome (← links)
- Polysomy (← links)
- Y chromosome microdeletion (← links)
- Extracellular signal-regulated kinases (← links)
- Acute lymphoblastic leukemia (← links)
- Interleukin-17 receptor (← links)
