High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome-Reference-Cited by-同舟云学术

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

Published:2005-12 Issue:6 Volume:26 Page:513-519
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Aretz Stefan,Stienen Dietlinde,Uhlhaas Siegfried,Loff Steffan,Back Walter,Pagenstecher Constanze,McLeod D. Ross,Graham Gail E.,Mangold Elisabeth,Santer René,Propping Peter,Friedl Waltraut

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. Genotype-phenotype correlations in Peutz-Jeghers syndrome

2. Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

3. Genetic heterogeneity in Peutz-Jeghers syndrome

4. Very high risk of cancer in familial Peutz–Jeghers syndrome

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