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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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Detalhes bibliográficos
Main Authors: Zhu, Junzhen, Cao, Qinying, Zhang, Ning, Zhao, Lijuan
Formato: Artigo
Idioma:Inglês
Publicado em: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2013
Assuntos:
Acesso em linha: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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