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 oncologyArticle was published in
Clinical Oncology
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