Kehrer-Sawatzki, H <br/><br/>
Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region.  [electronic resource] 

 -  Journal of medical genetics  Oct 2003 
 - e116 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.40.10.e116  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Animals<br/>Chromosome Breakage<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17<br/>Gene Order<br/>Genes, Neurofibromatosis 1<br/>Haplotypes<br/>Humans<br/>Male<br/>Mice<br/>Neurofibromatosis 1--genetics<br/>Synteny