Ballif, Blake C <br/><br/>
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.  [electronic resource] 

 -  Human genetics  Jan 2004 
 - 198-206 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s00439-003-1029-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Banding<br/>Chromosome Disorders<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 1--genetics<br/>Cytogenetic Analysis--methods<br/>DNA--genetics<br/>DNA Probes<br/>DNA Replication--genetics<br/>Gene Deletion<br/>Gene Rearrangement<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Monosomy--genetics<br/>Repetitive Sequences, Nucleic Acid--genetics<br/>Telomere--genetics<br/>Translocation, Genetic