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Cancer problem in Peutz–Jeghers syndrome

Peutz–Jeghers syndrome is a rare autosomal dominantly inherited condition, characterized by the presence of hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome can be associated with other neoplasms such as ovarian neoplasms known as sex-cord tumor with...

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Detaylı Bibliyografya
Asıl Yazarlar: Taheri, Diana, Afshar-Moghadam, Noushin, Mahzoni, Parvin, Eftekhari, Amin, Hashemi, Seyed Mozafar, Emami, Mohammad Hasan, Fesharakizadeh, Mehdi, Ghasemi-basir, Hamid Reza
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3748667/
https://ncbi.nlm.nih.gov/pubmed/23977663
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.109721
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