387 top medical experts on Uniparental Disomy across 40 countries and 38 U.S. states, including 212 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Uniparental Disomy: The presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent. This chromosome composition stems from non-disjunction (nondisjunction, genetic) events during meiosis. The disomy may be composed of both homologous chromosomes from one parent (heterodisomy) or a duplicate of one chromosome (isodisomy).
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Chromosome Aberrations (4,639), Genetic Nondisjunction (236).
- Clinical Trials : at least 1 including 1 Recruiting
- Synonyms: Uniparental Heterodisomy, Uniparental Isodisomy
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