Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15

Proceedings of the National Academy of Sciences of the United States of America

Volumn 89, Issue 17, 1992, Pages 7968-7972

  McDaniel, L D ^a   Schultz, R A ^a  

^a UNIVERSITY OF MARYLAND   (United States)

Author keywords

chromosome mapping; DNA repair; genetic complementation

Indexed keywords

ARTICLE; BLOOM SYNDROME; CHROMOSOME 15; CHROMOSOME MAP; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; FIBROBLAST CULTURE; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; LESCH NYHAN SYNDROME; NEOPLASM; PHENOTYPE; PRIORITY JOURNAL; SIMIAN VIRUS 40; SISTER CHROMATID EXCHANGE; VIRUS CELL TRANSFORMATION; XERODERMA PIGMENTOSUM;

SIMIAE; SIMIAN VIRUS; SIMIAN VIRUS 40;

EID: 0026732784     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.89.17.7968     Document Type: Article

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