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Prader-willi syndrome: A case report and a Chinese literature review
Prader-Willi syndrome (PWS) is a genetic disorder, resulting from lack of gene expression on the paternally inherited chromosome 15. It is important to determine diagnostic methods for PWS for early treatment. In this study, we report a newborn with Prader-willi syndrome. We further summarized the g...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4204554/ https://ncbi.nlm.nih.gov/pubmed/25343115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2013.v2.4.123 |
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