Search details
1.
Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.
Hum Mutat
; 33(12): 1647-55, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-22753075
2.
Characteristics of the Danish families with multiple endocrine neoplasia type 1.
Mol Cell Endocrinol
; 249(1-2): 123-32, 2006 Apr 25.
Article
in English
| MEDLINE | ID: mdl-16563611
3.
Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA.
Oncogene
; 23(7): 1457-68, 2004 Feb 19.
Article
in English
| MEDLINE | ID: mdl-14676842
4.
Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer.
Mutat Res
; 570(1): 89-96, 2005 Feb 15.
Article
in English
| MEDLINE | ID: mdl-15680406
5.
Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.
Hum Mutat
; 20(1): 20-7, 2002 Jul.
Article
in English
| MEDLINE | ID: mdl-12112654
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