The following pages link to Uniparental disomy
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Down syndrome (links | edit)
- Genetic disorder (links | edit)
- Genomic imprinting (links | edit)
- Mutation (links | edit)
- XYY syndrome (links | edit)
- Trisomy (links | edit)
- Turner syndrome (links | edit)
- Fragile X syndrome (links | edit)
- Inbreeding (links | edit)
- Prader–Willi syndrome (links | edit)
- List of diseases (U) (links | edit)
- Twin (links | edit)
- Chromosome 15q partial deletion (links | edit)
- Miscarriage (links | edit)
- Williams syndrome (links | edit)
- TAR syndrome (links | edit)
- Deletion (genetics) (links | edit)
- Multiple myeloma (links | edit)
- Aneuploidy (links | edit)
- Birth defect (links | edit)
- Burkitt lymphoma (links | edit)
- Genetic variation (links | edit)
- Consanguinity (links | edit)
- Patau syndrome (links | edit)
- Trisomy 18 (links | edit)
- Nondisjunction (links | edit)
- Philadelphia chromosome (links | edit)
- Chromosomal translocation (links | edit)
- Mosaic (genetics) (links | edit)
- Beckwith–Wiedemann syndrome (links | edit)
- Acute lymphoblastic leukemia (links | edit)
- Miller–Dieker syndrome (links | edit)
- Anaplastic large-cell lymphoma (links | edit)
- Wolf–Hirschhorn syndrome (links | edit)
- Dermatofibrosarcoma protuberans (links | edit)
- Acute promyelocytic leukemia (links | edit)
- Chromosome 5q deletion syndrome (links | edit)
- Cri du chat syndrome (links | edit)
- Monosomy (links | edit)
- Index of genetics articles (links | edit)
- Loss of heterozygosity (links | edit)
- Synovial sarcoma (links | edit)
- Jacobsen syndrome (links | edit)
- Small supernumerary marker chromosome (links | edit)
- Desmoplastic small-round-cell tumor (links | edit)
- Microtia (links | edit)
- UPD (links | edit)
- Ring chromosome (links | edit)
- Smith–Magenis syndrome (links | edit)
- Trisomy 8 (links | edit)