Low frequency of hMSH2 mutations in Swedish HNPCC families.

International journal of cancer. Journal international du cancer

Volumn 74, Issue 1, 1997, Pages 134-137

  Wahlberg, S S ^a   Nystrom Lahti M ^a   Kane, M F ^a   Kolodner, R D ^a   Peltomaki P ^a   Lindblom, A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; MICROSATELLITE DNA; MSH2 PROTEIN, HUMAN; ONCOPROTEIN; PRIMER DNA; PROTEIN MSH2;

COLORECTAL TUMOR; FAMILY; GENE FREQUENCY; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETICS; HUMAN; LETTER; METHODOLOGY; MUTATION; POINT MUTATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; RISK FACTOR; SWEDEN;

COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA PRIMERS; DNA-BINDING PROTEINS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FAMILY; GENE FREQUENCY; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); MICROSATELLITE REPEATS; MUTATION; MUTS HOMOLOG 2 PROTEIN; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PROTO-ONCOGENE PROTEINS; RISK FACTORS; SWEDEN;

EID: 0031579366     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19970220)74:1<134::AID-IJC22>3.0.CO;2-E     Document Type: Letter

References (0)