Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associatedMARK/Par1gene family as potential PJS candidates-Reference-Cited by-同舟云学术

Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associatedMARK/Par1gene family as potential PJS candidates

Published:2007-10-09 Issue:6 Volume:72 Page:568-573
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

de Leng WWJ,Jansen M,Carvalho R,Polak M,Musler AR,Milne ANA,Keller JJ,Menko FH,de Rooij FWM,Iacobuzio-Donahue CA,Giardiello FM,Weterman MAJ,Offerhaus GJA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00907.x/fullpdf

Reference33 articles.

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2. Very high risk of cancer in familial Peutz-Jeghers syndrome;Giardiello;Gastroenterology,2000

3. Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis;Jansen;Gut,2006

4. Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome;Lim;Br J Cancer,2003

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

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