The following pages link to Chromosome 1
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Autosome (links | edit)
- Chromosome (links | edit)
- Charcot–Marie–Tooth disease (links | edit)
- DNA (links | edit)
- Down syndrome (links | edit)
- Mutation (links | edit)
- Nucleic acid (links | edit)
- XYY syndrome (links | edit)
- Trisomy (links | edit)
- Dalton (unit) (links | edit)
- Human genome (links | edit)
- Turner syndrome (links | edit)
- Biology and sexual orientation (links | edit)
- Fragile X syndrome (links | edit)
- Prader–Willi syndrome (links | edit)
- Mitochondrial DNA (links | edit)
- Miscarriage (links | edit)
- Adenosine monophosphate deaminase deficiency type 1 (links | edit)
- Progeria (links | edit)
- X chromosome (links | edit)
- Williams syndrome (links | edit)
- TAR syndrome (links | edit)
- Factor V Leiden (links | edit)
- Deletion (genetics) (links | edit)
- Y chromosome (links | edit)
- Sarcoma (links | edit)
- Multiple myeloma (links | edit)
- Aneuploidy (links | edit)
- Birth defect (links | edit)
- Uniparental disomy (links | edit)
- Burkitt lymphoma (links | edit)
- Patau syndrome (links | edit)
- Spinal muscular atrophies (links | edit)
- Trisomy 18 (links | edit)
- Atrial natriuretic peptide (links | edit)
- Philadelphia chromosome (links | edit)
- Chromosomal translocation (links | edit)
- Satellite DNA (links | edit)
- Mosaic (genetics) (links | edit)
- Beckwith–Wiedemann syndrome (links | edit)
- Acute lymphoblastic leukemia (links | edit)
- Primary familial brain calcification (links | edit)
- Osteogenesis imperfecta (links | edit)
- Miller–Dieker syndrome (links | edit)
- Alkaline phosphatase (links | edit)
- Usher syndrome (links | edit)
- Duffy antigen system (links | edit)
- Anaplastic large-cell lymphoma (links | edit)
- Wolf–Hirschhorn syndrome (links | edit)
- Dermatofibrosarcoma protuberans (links | edit)