Näf, D <br/><br/>
Mouse models for the Wolf-Hirschhorn deletion syndrome.  [electronic resource] 

 -  Human molecular genetics  Jan 2001 
 - 91-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/10.2.91  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Animals<br/>Brain--abnormalities<br/>Chimera--genetics<br/>Craniofacial Abnormalities--genetics<br/>Disease Models, Animal<br/>Eye Abnormalities--genetics<br/>Genetic Linkage<br/>Growth Disorders--genetics<br/>Haploidy<br/>Humans<br/>Huntington Disease--genetics<br/>Intellectual Disability--genetics<br/>Mice<br/>Mice, Inbred C3H<br/>Mice, Inbred C57BL<br/>Mice, Neurologic Mutants<br/>Phenotype<br/>Seizures--genetics<br/>Sequence Deletion<br/>Syndrome