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Correlation between genotype and phenotype in three families with Peutz-Jeghers Syndrome
Peutz-Jeghers syndrome (PJS) is a hereditary disorder characterized by mucocutaneous pigmentations, gastrointestinal (GI) polyposis and an increased risk of certain malignancies. Little is known about the causative genes of PJS, or their association with the clinical phenotypes of PJS. The present s...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5348679/ https://ncbi.nlm.nih.gov/pubmed/28352323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2016.3980 |
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