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1.
Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC).
Hum Mutat
; 27(4): 388, 2006 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-16541406
2.
The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing alone.
Fam Cancer
; 5(1): 21-8, 2006.
Artículo
en Inglés
| MEDLINE | ID: mdl-16528605
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