Nasal polyposis in Peutz–Jeghers syndrome: a distinct histopathological and molecular genetic entity

BACKGROUND: Peutz–Jeghers syndrome (PJS) is an autosomal dominant hamartomatous polyposis syndrome of the gastrointestinal tract, caused by a germline STK11/LKB1 mutation. Nasal polyposis was described in the original report by Peutz. Recently, a molecular–genetic association between nasal polyposis...

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Detalhes bibliográficos
Main Authors: de Leng, Wendy W J, Westerman, Anne Marie, Weterman, Marian A J, Jansen, Marnix, van Dekken, Herman, Giardiello, Francis M, de Rooij, Felix W M, Wilson, J H Paul, Offerhaus, G Johan A, Keller, Josbert J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2001113/
https://ncbi.nlm.nih.gov/pubmed/16775120
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jcp.2005.036418
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