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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Detalles Bibliográficos
Autores principales: Zhang, Yanli, Ke, Yao, Zheng, Xueni, Liu, Qing, Duan, Xiaohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348679/
https://www.ncbi.nlm.nih.gov/pubmed/28352323
http://dx.doi.org/10.3892/etm.2016.3980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348679/
https://www.ncbi.nlm.nih.gov/pubmed/28352323
http://dx.doi.org/10.3892/etm.2016.3980

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