Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype

Human Genetics

Volumn 97, Issue 2, 1996, Pages 176-179

  Itoh, Toshiki ^a   Cleaver, James E ^b   Yamaizumi, Masaru ^a  

^a KUMAMOTO UNIVERSITY   (Japan)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; RNA;

ARTICLE; CASE REPORT; CELL FUSION; COCKAYNE SYNDROME; CONTROLLED STUDY; FIBROBLAST; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; PHENOTYPE; PRIORITY JOURNAL; RADIOSENSITIVITY; RNA SYNTHESIS; ULTRAVIOLET RADIATION; UNSCHEDULED DNA SYNTHESIS; XERODERMA PIGMENTOSUM;

CELL FUSION; CELLS, CULTURED; COCKAYNE SYNDROME; DNA; DNA REPAIR; FIBROBLASTS; GENETIC COMPLEMENTATION TEST; HUMANS; PHENOTYPE; RADIATION TOLERANCE; RNA; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0030060577     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02265261     Document Type: Article

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