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PMS2
LE WE PMID CA
PMS211797PMS2

Colon and rectum (Neoplasia)

Genetics (Microsatellite)

Lynch syndrome

MLH1

MSH2

MSH6

Neoplasia (Inherited)

PMS2

2008  
1
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
[18602922] Gastroenterology 135(2): 419-28 (2008)
2010  
2
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
[20587412] J Med Genet 47(9): 579-85 (2010)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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