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Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome
Prader-willi syndrome (PWS) is the most common form of dysmorphic genetic obesity associated with mental retardation(1,2). About 60% of cases have a cytological deletion of chromosome 15q11q13 (refs 2, 3). These deletions occur de novo exclusively on the paternal chromosome(4,5). By contrast, Angelm...
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| Veröffentlicht in: | Nature |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
1989
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6706849/ https://ncbi.nlm.nih.gov/pubmed/2812027 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/342281a0 |
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