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Results 1 - 10 of 11 for Maternal uniparental disomy of chromosome 20
Did you mean Maternal uniparental trisomy of chromosome 20?
  1. Chromosome 14 
    ... Curtis CA, Bass NE, Zinn AB, Schwartz S. Maternal uniparental disomy chromosome 14: case report and literature review. Pediatr Neurol. 2005 Feb;32(2):116-20. doi: 10.1016/j.pediatrneurol.2004.07.007. ...
    https://medlineplus.gov/genetics/chromosome/14 - Genetics
  2. Angelman syndrome 
    ... is deleted. In other cases (about 10 to 20 percent), Angelman syndrome is caused ... uniparental disomy. Rarely, Angelman syndrome can also be caused by ...
    https://medlineplus.gov/genetics/condition/angelman-syndrome - Genetics
  3. FOXG1 gene 
    ... mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14. Am J Med Genet A. 2011 Oct; ...
    https://medlineplus.gov/genetics/gene/foxg1 - Genetics
  4. Prader-Willi syndrome 
    ... those caused by a deletion in the paternal chromosome 15 or by maternal uniparental disomy. These genetic changes occur as random events during ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  5. Chromosome 7 
    ... a translocation) or from inheriting two copies of chromosome 7 from the mother instead of one from each parent (a phenomenon called maternal uniparental disomy or maternal UPD, which is described in more ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  6. Chromosome 6 
    ... copy of each gene that comes from the mother is inactivated (silenced) by a ... disomy (UPD) of chromosome 6. In paternal UPD, people inherit both copies ...
    https://medlineplus.gov/genetics/chromosome/6 - Genetics
  7. Chromosome 11 
    ... caused by a genetic change known as paternal uniparental disomy (UPD). ... the chromosome. In people with Beckwith-Wiedemann syndrome, paternal UPD ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
  8. PLAGL1 gene 
    ... caused by a genetic change known as paternal uniparental disomy (UPD) of ... inactive copy from the mother.Another 40 percent of cases of 6q24-related ...
    https://medlineplus.gov/genetics/gene/plagl1 - Genetics
  9. 6q24-related transient neonatal diabetes mellitus 
    ... caused by a genetic change known as paternal uniparental disomy (UPD) of ... inactive copy from the mother.Another 40 percent of cases of 6q24-related ...
    https://medlineplus.gov/...ated-transient-neonatal-diabetes-mellitus - Genetics
  10. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Genetic Testing/Reference Desk ... Genetic Testing ... Newborn Screening/Reference Desk ... Newborn Screening ... National Center for Biotechnology Information ... From the National ...
    https://www.ncbi.nlm.nih.gov/books/NBK5191 - External Health Links
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