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Is gestation in Prader-Willi syndrome affected by the genetic subtype?
BACKGROUND: Prader-Willi syndrome (PWS) is a complex genetic disorder with errors in genomic imprinting, generally due to a paternal deletion of chromosome 15q11-q13 region. Maternal disomy 15 (both 15s from the mother) is the second most common form of PWS resulting from a trisomic zygote followed...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer US
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2767487/ https://ncbi.nlm.nih.gov/pubmed/19760168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-009-9341-7 |
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