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Maternal uniparental trisomy of chromosome 20
- ... 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. ...
- GeneReviews Glossary (National Center for Biotechnology Information)Newborn Screening/Reference Desk ... Newborn Screening ... Genetic Testing/Reference Desk ... Genetic Testing ... National Center for Biotechnology Information ... From the National ...
- ... 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 ...
- ... other characteristic features of Beckwith-Wiedemann syndrome.About 20 percent ... copy from the mother. People with paternal UPD are also missing genes ...
- ... part of chromosome 15 in each cell (partial trisomy 15), a missing segment of the chromosome in each cell (partial monosomy 15), and a ... G. Partial duplication of the long arm of chromosome 15: confirmation of a ... definition of a 15q25-qter trisomy syndrome. Am J Med Genet. 1999 Dec 22; ...