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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...
Kaydedildi:
| Yayımlandı: | Am J Med Genet A |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2008
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| Konular: | |
| Online Erişim: | 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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