#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Peutz-Jeghers Syndrome


Authors: A. Puchmajerová;  P. Vasovčák;  A. Křepelová
Authors‘ workplace: Ústav biologie a lékařské genetiky FN Motol a 2. LF UK, Praha
Published in: Klin Onkol 2009; 22(Supplementum): 36-37


Sources

1. Amos CI, Frazier ML, McGarrity TJ et al. Peutz-Jeghers Syndrome. GeneReviews 2007. Dostupné z http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pjs.

2. Aretz S, Stienen D, Uhlhaas S et al. High Proportion of Large Genomic STK11 Deletions in Peutz-Jeghers Syndrome. Human Mutation 2005; 26(6): 513–519.

3. Hearle NCM, Rudd MF, Lim W et al. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. J Med Genet 2006; 43: e15.

4. Tomlinson IPM, Houlston RS. Peutz-Jeghers syndrome. J Med Genet 1997; 34: 1007–1011.

Labels
Paediatric clinical oncology Surgery Clinical oncology
Topics Journals
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#