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Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review)
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease that is characterized by gastrointestinal hamartomatous polyposis and mucocutaneous melanin spots. The tumor suppressor gene, STK11/LKB1, which is located on chromosome 19p13.3, has been reported to be responsible for this condition. PJS...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
D.A. Spandidos
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3813608/ https://ncbi.nlm.nih.gov/pubmed/24179492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2013.1527 |
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