Identification of a one-base germline deletion (Codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2

Human Mutation

Volumn 10, Issue 1, 1997, Pages 80-81

  Swensen, Jeff ^a   Lewis, Cathryn M ^a   Cannon Albright, Lisa A ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER GENETICS; CLINICAL ARTICLE; COLORECTAL CANCER; DNA POLYMORPHISM; GENE DELETION; GENE MUTATION; HUMAN; INTRON; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA REPAIR; DNA-BINDING PROTEINS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; GENETIC SCREENING; GERM-LINE MUTATION; HUMANS; LINKAGE DISEQUILIBRIUM; MUTS HOMOLOG 2 PROTEIN; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PROTO-ONCOGENE PROTEINS; RNA SPLICING; SEQUENCE DELETION;

EID: 0030802503     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1997)10:1<80::AID-HUMU12>3.0.CO;2-W     Document Type: Article

References (9)

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