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Array Comparative Genomic Hybridization (aCGH) Analysis in Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is due to loss of paternally expressed genes in the 15q11–q13 region generally from a paternal 15q11–q13 deletion. The proximal deletion breakpoint in the 15q11–q13 region occurs at one of two sites located within either of two large duplicons allowing for identification...
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| Vydáno v: | Am J Med Genet A |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438264/ https://ncbi.nlm.nih.gov/pubmed/18266248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32249 |
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