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Results 1 - 8 of 8 for Maternal uniparental disomy of chromosome 14
  1. ... Curtis CA, Bass NE, Zinn AB, Schwartz S. Maternal uniparental disomy chromosome 14: case report and literature review. Pediatr Neurol. 2005 ... Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14. Epigenetics. 2008 Jul-Aug;3(4):181-7. ...
  2. ... mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14. Am J Med Genet A. 2011 Oct;155A( ...
  3. ... those caused by a deletion in the paternal chromosome 15 or by maternal uniparental disomy. These genetic changes occur as random events during ...
  4. ... one from each parent (a phenomenon called maternal uniparental disomy or maternal UPD). It remains unclear how having two maternal copies of chromosome 7 affects the activity of the FOXP2 gene. ...
  5. ... 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 ...
  6. ... parts of the brain, a deletion in the maternal chromosome 15 leaves no active ... uniparental disomy (UPD). People with paternal UPD for chromosome 15 ...
  7. ... caused by a genetic change known as paternal uniparental disomy (UPD). ... chromosome. In Beckwith-Wiedemann syndrome, paternal UPD usually occurs ...
  8. 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 ...