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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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Detaylı Bibliyografya
Asıl Yazarlar: Zhu, Junzhen, Cao, Qinying, Zhang, Ning, Zhao, Lijuan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2013
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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