MSH2 genomic deletions are a frequent cause of HNPCC [2]

Nature Genetics

Volumn 20, Issue 4, 1998, Pages 326-328

  Wijnen, J ^a   Van der Klift, H ^a   Vasen, H F A ^a   Khan, P M ^a   Menko, F ^a   Tops, C ^a   Heijboer, H M ^a   Lindhout, D ^a   Moller, P ^a   Fodde, R ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; BASE MISPAIRING; CANCER SUSCEPTIBILITY; COLORECTAL CANCER; GENE DELETION; GENE MUTATION; GENETIC PREDISPOSITION; HYBRIDIZATION; LETTER; PRIORITY JOURNAL;

BASE PAIR MISMATCH; BASE SEQUENCE; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA-BINDING PROTEINS; EXONS; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MUTS HOMOLOG 2 PROTEIN; PROTO-ONCOGENE PROTEINS;

EID: 0031795020     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/3795     Document Type: Letter

References (16)