Identification of molecular alterations in gastrointestinal carcinomas and dysplastic hamartomas in Peutz-Jeghers syndrome-Reference-Cited by-同舟云学术

Identification of molecular alterations in gastrointestinal carcinomas and dysplastic hamartomas in Peutz-Jeghers syndrome

Published:2013-02-20 Issue:7 Volume:34 Page:1611-1619
ISSN:1460-2180
Container-title:Carcinogenesis
language:en
Short-container-title:

Author:

Korsse Susanne E.,Biermann Katharina,Offerhaus G.Johan A.,Wagner Anja,Dekker Evelien,Mathus-Vliegen Elisabeth M.H.,Kuipers Ernst J.,van Leerdam Monique E.,van Veelen Wendy

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,General Medicine

Link

http://academic.oup.com/carcin/article-pdf/34/7/1611/17295434/bgt068.pdf

Reference27 articles.

1. Peutz-Jeghers syndrome and management recommendations;Giardiello;Clin. Gastroenterol. Hepatol,(2006)

2. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome;Hemminki;Nature,(1998)

3. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase;Jenne;Nat. Genet,(1998)

4. LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome;Volikos;J. Med. Genet,(2006)

5. Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates;de Leng;Clin. Genet,(2007)

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