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Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
The Prader-Willi syndrome (PWS) is a human imprinting disorder resulting from genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. This genetic condition appears to be a contiguous gene syndrome caused by the loss of at least 2 of a number o...
保存先:
| 出版年: | Ann Pediatr Endocrinol Metab |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Korean Society of Pediatric Endocrinology
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5073158/ https://ncbi.nlm.nih.gov/pubmed/27777904 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2016.21.3.126 |
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