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                                       Details for article 17 of 25 found articles
 
 
  MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation
 
 
Title: MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation
Author: Nguyen, Aurélia
Bougeard, Gaelle
Koob, Meriam
Chenard, Marie Pierre
Schneider, Anne
Maugard, Christine
Entz-Werle, Natacha
Appeared in: Familial cancer
Paging: Volume 15 (2016) nr. 4 pages 571-577
Year: 2016
Contents:
Publisher: Springer Netherlands, Dordrecht
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 17 of 25 found articles
 
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