Identification of a novel PTEN intronic deletion in Li-Fraumeni syndrome and its effect on RNA processing

Cancer Genetics and Cytogenetics

Volumn 123, Issue 1, 2000, Pages 65-68

  Brown, Lauren T R ^a,b   Sexsmith, Elizabeth ^a   Malkin, David ^a,b  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FAMILIAL CANCER; GENE DELETION; HUMAN; HUMAN CELL; INTRON; LYMPHOCYTE; MUTATION; PRIORITY JOURNAL; RNA PROCESSING; SINGLE STRAND CONFORMATION POLYMORPHISM; TUMOR SUPPRESSOR GENE;

BASE SEQUENCE; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GERM-LINE MUTATION; HUMANS; INTRONS; LI-FRAUMENI SYNDROME; MALE; PEDIGREE; PHOSPHORIC MONOESTER HYDROLASES; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PTEN PHOSPHOHYDROLASE; RNA PROCESSING, POST-TRANSCRIPTIONAL; RNA, MESSENGER; SEQUENCE DELETION; TUMOR SUPPRESSOR PROTEINS;

EID: 0033668977     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(00)00303-4     Document Type: Article

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