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A twin sibling with Prader-Willi syndrome caused by type 2 microdeletion following assisted reproductive technology: A case report
Prader-Willi syndrome (PWS) is a neurobehavioral imprinting disorder, which arises due to an absence of paternally expressed genes within the 15q11.2-q13 region. This occurs via one of the three main genetic mechanisms, as follows: Deletion of the paternally inherited 15q11.2-q13 region, maternal un...
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| Vydáno v: | Biomed Rep |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
D.A. Spandidos
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4906703/ https://ncbi.nlm.nih.gov/pubmed/27330749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2016.675 |
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