Potocki, L <br/><br/>
Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.  [electronic resource] 

 -  Nature genetics  Jan 2000 
 - 84-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/71743  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Genotype<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Male<br/>Pedigree<br/>Recombination, Genetic<br/>Syndrome