Bogani, Debora <br/><br/>
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Aug 2005 
 - 12477-82 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.0500584102  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Anophthalmos--genetics<br/>Brain--abnormalities<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 6--genetics<br/>Congenital Abnormalities--genetics<br/>Craniofacial Abnormalities--genetics<br/>Female<br/>Genes, Lethal<br/>Genes, Recessive<br/>Genetic Testing--methods<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Kidney--abnormalities<br/>Male<br/>Mice<br/>Mice, Inbred C3H<br/>Mice, Inbred C57BL<br/>Mice, Mutant Strains<br/>Multigene Family<br/>Mutation<br/>Phenotype<br/>Species Specificity<br/>Syndrome