Sakamoto Hojo, E T <br/><br/>
Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique.  [electronic resource] 

 -  Mutation research  Feb 1995 
 - 59-69 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0027-5107 
<br/><br/><label>Standard No.: </label>10.1016/0165-1161(95)90031-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ataxia Telangiectasia--genetics<br/>Bloom Syndrome--genetics<br/>Cell Line<br/>Cell Line, Transformed<br/>Chromosome Aberrations<br/>Fanconi Anemia--genetics<br/>Fibroblasts--ultrastructure<br/>Gene Library<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Lymphocytes--ultrastructure<br/>Microscopy, Fluorescence<br/>Simian virus 40<br/>Sister Chromatid Exchange