Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in...

Cancer Letters 2007 Vol. 248; Iss. 1

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations

Steffen Pistorius, Heike Görgens, Jens Plaschke, Ruth Hoehl, Stefan Krüger, Christoph Engel, Hans-Detlev Saeger, Hans K. Schackert
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Volume:
248
Year:
2007
Language:
english
Pages:
96
DOI:
10.1016/j.canlet.2006.06.002
File:
PDF, 495 KB
english, 2007
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