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Maternal uniparental disomy of chromosome 14
Did you mean Maternal uniparental trisomy of chromosome 14?
- ... 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. ...
- ... mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14. Am J Med Genet A. 2011 Oct;155A( ...
- ... those caused by a deletion in the paternal chromosome 15 or by maternal uniparental disomy. These genetic changes occur as random events during ...
- ... 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. ...
- ... 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 ...
- ... parts of the brain, a deletion in the maternal chromosome 15 leaves no active ... uniparental disomy (UPD). People with paternal UPD for chromosome 15 ...
- ... caused by a genetic change known as paternal uniparental disomy (UPD). ... chromosome. In Beckwith-Wiedemann syndrome, paternal UPD usually occurs ...
- Genetic Testing/Reference Desk ... Genetic Testing ... Newborn Screening/Reference Desk ... Newborn Screening ... National Center for Biotechnology Information ... From the National ...