Probst, F J <br/><br/>
A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2).  [electronic resource] 

 -  Genomics  Feb 1999 
 - 348-52 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.1998.5669  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Animals<br/>Chromosomes, Artificial, Yeast<br/>Chromosomes, Human, Pair 17--genetics<br/>DNA Primers<br/>Disease Models, Animal<br/>Gene Deletion<br/>Humans<br/>Intellectual Disability--genetics<br/>Mice<br/>Models, Genetic<br/>Molecular Sequence Data<br/>Myosins--genetics<br/>Physical Chromosome Mapping<br/>Sequence Tagged Sites<br/>Syndrome